Joseph Epstein Food Enterprises, Inc. Recalls Gluten-Free Turkey Meatball Products Due to Misbranding
Class II Recall 134-2015
Health Risk: Low Oct 30, 2015
Congressional and Public Affairs
Kristen Felicione
(202) 720-9113
WASHINGTON, Oct. 30, 2015 – Joseph Epstein Food Enterprises, Inc., an East Rutherford, N.J. establishment, is recalling approximately 190 pounds of turkey meatball products due to misbranding, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The label declares the product as “gluten-free,” a false negative claim.
The Mama Mancini’s gluten-free turkey meatball items were produced on Oct. 19, 2015. The following products are subject to recall: [View Labels]
22-oz. cartons of “Mama Mancini’s Slow Cooked Italian Style Sauce and Turkey Meatballs – Gluten Free.”
The products subject to recall bear establishment number “P-21734” inside the USDA mark of inspection, product code 4740 and expiration date “Use by 12/10/15.” These items were shipped to retail locations in New Jersey.
The problem was discovered during the establishment’s third party laboratory testing; the product was found to contain an excess of the maximum allowable 20 ppm of gluten. The establishment notified FSIS of the problem.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact Mr. Matt Brown, President, at (917) 705-7514. Media with questions about the recall can contact Mr. Carl Wolf at (973) 985-0280.
Friday, October 30, 2015
New #foodsafety #recall of Pelman foods products produced without the benefit of inspection
Pelmen Foods Recalls Beef, Chicken and Pork Products Produced Without Benefit of Import Inspection
Class I Recall 133-2015
Health Risk: High Oct 30, 2015
Congressional and Public Affairs
Alexandra Tarrant
(202) 720-9113
WASHINGTON, Oct. 30, 2015 - Pelmen Foods, an Ontario, Canada, establishment, is recalling approximately 332 pounds of beef, chicken and pork dumpling products that were not presented at the U.S. point of entry for inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Without the benefit of full inspection, a possibility of adverse health consequences exists.
The dumpling products were imported on Oct. 8, 2015. The following products, sold between Oct. 8, 2015 and Oct. 30, 2015, are subject to recall: [View Labels (PDF Only)]
12.4 lb. cases containing 12 bags of “Pelmen Foods PELMENI Siberian Recipe (Pork & Beef)” with “EXP Oct 02’ 16” and Lot 5275 on the bags
12.4 lb. cases containing 12 bags of “Pelmen Foods PELMENI Chicken” with “EXP Oct 02’ 16” and Lot 5275 on the bags
The products subject to recall bear establishment number “721” inside Canada’s mark of inspection. These items were shipped to distributors in Illinois and Wisconsin.
The problem was discovered during routine FSIS surveillance activities of imported products.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and media with questions about the recall can contact Svetlana Minos, Quality Assurance and HACCP Coordinator, at (416) 661-9600 Ext 205.
Class I Recall 133-2015
Health Risk: High Oct 30, 2015
Congressional and Public Affairs
Alexandra Tarrant
(202) 720-9113
WASHINGTON, Oct. 30, 2015 - Pelmen Foods, an Ontario, Canada, establishment, is recalling approximately 332 pounds of beef, chicken and pork dumpling products that were not presented at the U.S. point of entry for inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Without the benefit of full inspection, a possibility of adverse health consequences exists.
The dumpling products were imported on Oct. 8, 2015. The following products, sold between Oct. 8, 2015 and Oct. 30, 2015, are subject to recall: [View Labels (PDF Only)]
12.4 lb. cases containing 12 bags of “Pelmen Foods PELMENI Siberian Recipe (Pork & Beef)” with “EXP Oct 02’ 16” and Lot 5275 on the bags
12.4 lb. cases containing 12 bags of “Pelmen Foods PELMENI Chicken” with “EXP Oct 02’ 16” and Lot 5275 on the bags
The products subject to recall bear establishment number “721” inside Canada’s mark of inspection. These items were shipped to distributors in Illinois and Wisconsin.
The problem was discovered during routine FSIS surveillance activities of imported products.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and media with questions about the recall can contact Svetlana Minos, Quality Assurance and HACCP Coordinator, at (416) 661-9600 Ext 205.
New #foodsafety #recall undeclared #allergen of Soy in Natures Promise Organic Edamame
Stop & Shop Alerts Customers To Voluntary Recall Of Nature's Promise Organic Edamame
Consumers: Stop & Shop Customer Service 1-800-767-7772
Purchase, NY & Quincy, MA – The Stop & Shop Supermarket Company LLC announced it removed from sale Nature’s Promise Organic Edamame products because they contain soy, which is not listed on the ingredient label. These products are safe to consume for individuals who do not suffer from a soy allergy.
The following products are included in this recall:
Nature’s Promise Organic Shelled Edamame, 16 oz., UPC 68826712764
Nature’s Promise Organic Edamame in Pod, 16 oz., UPC 68826702124
Stop & Shop has received no reports of illnesses to date. People who have an allergy or severe sensitivity to soy may run the risk of serious or life-threatening allergic reaction if they consume these products. Symptoms of food allergies typically appear from within a few minutes to two hours after a person has eaten the food to which he or she is allergic. Allergic reactions can include: hives; flushed skin or rash; tingling or itchy sensation in the mouth; face, tongue, or lip swelling; vomiting and/or diarrhea; abdominal cramps; coughing or wheezing; dizziness and/or lightheadedness; swelling of the throat and vocal cords; difficulty breathing; loss of consciousness.
Customers who have purchased these products should discard any unused portions and bring their purchase receipt to Stop & Shop for a full refund.
Consumers looking for additional information on the recall may call Stop & Shop Customer Service at 1-800-767-7772 for more information. Customers can also visit the Stop & Shop website at stopandshop.com
The Stop & Shop Supermarket Company LLC employs over 59,000 associates and operates 395 stores throughout Massachusetts, Connecticut, Rhode Island, New York and New Jersey. The company helps support local communities fight hunger, combat childhood cancer and promote general health and wellness – with emphasis on children’s educational and support programs. In its commitment to be a sustainable company, Stop & Shop is a member of the U.S. Green Building Council and EPA’s Smart Way program and has been recognized by the EPA for the superior energy management of its stores. Stop & Shop is an Ahold company. To learn more about Stop & Shop, visit www.stopandshop.com or www.facebook.com/stopandshop.
Consumers: Stop & Shop Customer Service 1-800-767-7772
Purchase, NY & Quincy, MA – The Stop & Shop Supermarket Company LLC announced it removed from sale Nature’s Promise Organic Edamame products because they contain soy, which is not listed on the ingredient label. These products are safe to consume for individuals who do not suffer from a soy allergy.
The following products are included in this recall:
Nature’s Promise Organic Shelled Edamame, 16 oz., UPC 68826712764
Nature’s Promise Organic Edamame in Pod, 16 oz., UPC 68826702124
Stop & Shop has received no reports of illnesses to date. People who have an allergy or severe sensitivity to soy may run the risk of serious or life-threatening allergic reaction if they consume these products. Symptoms of food allergies typically appear from within a few minutes to two hours after a person has eaten the food to which he or she is allergic. Allergic reactions can include: hives; flushed skin or rash; tingling or itchy sensation in the mouth; face, tongue, or lip swelling; vomiting and/or diarrhea; abdominal cramps; coughing or wheezing; dizziness and/or lightheadedness; swelling of the throat and vocal cords; difficulty breathing; loss of consciousness.
Customers who have purchased these products should discard any unused portions and bring their purchase receipt to Stop & Shop for a full refund.
Consumers looking for additional information on the recall may call Stop & Shop Customer Service at 1-800-767-7772 for more information. Customers can also visit the Stop & Shop website at stopandshop.com
The Stop & Shop Supermarket Company LLC employs over 59,000 associates and operates 395 stores throughout Massachusetts, Connecticut, Rhode Island, New York and New Jersey. The company helps support local communities fight hunger, combat childhood cancer and promote general health and wellness – with emphasis on children’s educational and support programs. In its commitment to be a sustainable company, Stop & Shop is a member of the U.S. Green Building Council and EPA’s Smart Way program and has been recognized by the EPA for the superior energy management of its stores. Stop & Shop is an Ahold company. To learn more about Stop & Shop, visit www.stopandshop.com or www.facebook.com/stopandshop.
New #foodsafety #recall possible #botulism contamination of Farmer Creek canned Albacore Tuna Products
Farmer Creek is Issuing a Voluntary Recall on Canned Albacore Tuna Products because of a Possible Health Risk
Consumers: porterrockproducts@gmail.com or 503-812-3793
Farmer Creek of Cloverdale, OR is voluntarily recalling canned albacore tuna with the Farmer Creek brand label with any codes starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
There have been no reported cases of illness to date.
All products were sold to consumers from our farm stand and farmers markets in Oregon. The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with "OC". The code can be found either on the bottom or on top of the can. Recalled product is packaged in metal cans with net weight of 6oz.
This voluntary recall was initiated after we were notified that our products were possibly under-processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers are advised to destroy recalled product.
If you have any questions, please contact Farmer Creek by email to porterrockproducts@gmail.com
Consumers: porterrockproducts@gmail.com or 503-812-3793
Farmer Creek of Cloverdale, OR is voluntarily recalling canned albacore tuna with the Farmer Creek brand label with any codes starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
There have been no reported cases of illness to date.
All products were sold to consumers from our farm stand and farmers markets in Oregon. The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with "OC". The code can be found either on the bottom or on top of the can. Recalled product is packaged in metal cans with net weight of 6oz.
This voluntary recall was initiated after we were notified that our products were possibly under-processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers are advised to destroy recalled product.
If you have any questions, please contact Farmer Creek by email to porterrockproducts@gmail.com
New #foodsafety #recall possible #listeria, #salmonella, and/or #Ecoli contamination of Northstar Produce Granny Smith Apples
Northstar Produce Inc. Recalls Granny Smith Size 175 Apples Because of Possible Health Risk
Consumers: Mike Abernathy 763-286-0110
Northstar Produce Inc.ofSt. Louis Park, MNthe presence of Listeria monocytogenes, Salmonella, and / or Enterohemorrhagic E. coli. is recalling 33 cases of Granny Smith Size 175ct apples, because a test performed on a sample of the apples indicated the presence of Listeria monocytogenes, Salmonella, and / or Enterohemorrhagic E. coli.
Salmonella, is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Listeria monocytogenes, is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Enterohemorrhagic E. coli is a bacteria that causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death.
The Granny Smith Size 175ct apples were sold at Mike’s Discount Foods, 230 Osborn Ave., Fridley, MN and Mikes’s Discount Foods, 516 East River Road, Anoka, MN
The apples were sold in tray packs between October 1, 2015 and October 19, 2015
No illnesses have been reported to date.
Consumers who purchased these apples should directly contact Mike Abernathy at 763-286-0110.
Consumers: Mike Abernathy 763-286-0110
Northstar Produce Inc.ofSt. Louis Park, MNthe presence of Listeria monocytogenes, Salmonella, and / or Enterohemorrhagic E. coli. is recalling 33 cases of Granny Smith Size 175ct apples, because a test performed on a sample of the apples indicated the presence of Listeria monocytogenes, Salmonella, and / or Enterohemorrhagic E. coli.
Salmonella, is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Listeria monocytogenes, is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Enterohemorrhagic E. coli is a bacteria that causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death.
The Granny Smith Size 175ct apples were sold at Mike’s Discount Foods, 230 Osborn Ave., Fridley, MN and Mikes’s Discount Foods, 516 East River Road, Anoka, MN
The apples were sold in tray packs between October 1, 2015 and October 19, 2015
No illnesses have been reported to date.
Consumers who purchased these apples should directly contact Mike Abernathy at 763-286-0110.
New #foodsafety #recall possible foreign material in certain packages of Kar's Nuts Sweet 'N Salty Mix
Kar's Nuts Recalling Certain Packages of Sweet 'N Salty Mix
Consumers: Molly Titcombe
mtitcombe@karsnuts.com or 800-527-6887
Kar’s Nuts, Inc. announces it has recalled a limited number of packages of their Sweet n Salty Mix products with best by dates between August 25, 2016 and September 2, 2016.
The recall is being initiated due to consumer reports of hard, clear foreign material (approximately one half the size of a sunflower kernel) being found in several packages. There are no reports of injury.
All recalled product is being removed from store shelves.
Consumers who have purchased the product with the best by dates in question can return it to its place of purchase for a full refund. Consumers with any questions may contact the company at 800-527-6887.
The list of specific items and their UPC codes will appear on the company’s website at karsnuts.com and also on the FDA website.
We value and appreciate the many consumers who purchase our products on a daily basis and consider us a favorite. We are committed to maintaining your trust and doing whatever it takes to ensure that our snacks are safe and enjoyable.
Consumers: Molly Titcombe
mtitcombe@karsnuts.com or 800-527-6887
Kar’s Nuts, Inc. announces it has recalled a limited number of packages of their Sweet n Salty Mix products with best by dates between August 25, 2016 and September 2, 2016.
The recall is being initiated due to consumer reports of hard, clear foreign material (approximately one half the size of a sunflower kernel) being found in several packages. There are no reports of injury.
All recalled product is being removed from store shelves.
Consumers who have purchased the product with the best by dates in question can return it to its place of purchase for a full refund. Consumers with any questions may contact the company at 800-527-6887.
The list of specific items and their UPC codes will appear on the company’s website at karsnuts.com and also on the FDA website.
We value and appreciate the many consumers who purchase our products on a daily basis and consider us a favorite. We are committed to maintaining your trust and doing whatever it takes to ensure that our snacks are safe and enjoyable.
Thursday, October 29, 2015
New #foodsafety #recall possible metal pieces in limited number of Skippy Reduced Fat Peanut Butter.
Hormel Foods Sales LLC Voluntarily Recalls a Limited Number of Jars of Skippy Reduced Fat Creamy Peanut Butter Spread Due to Possible Metal Pieces
Consumers: Hormel Foods Customer Relations: 1-866-475-4779
Hormel Foods Sales LLC is voluntarily recalling 153 cases, or 1,871 total pounds, of a single code date of SKIPPY® Reduced Fat Creamy Peanut Butter Spread, due to the possibility that some jars may contain small pieces of metal shavings which were discovered on an in-line magnet check during routine cleaning. Foodborne objects that are greater than 7mm in length may cause injury such as severe choking with airway obstruction, gastrointestinal peroration or secondary infection. The recalled product is limited to 16.3 ounce jars with a "Best If Used By" date of DEC1416LR1 with a package UPC code of 37600-10500. The code date is located on top of the lid. A photo of the product and "Best If Used By" date appears below. Recalled product was sent to distribution centers for Publix, Target and Walmart located in Georgia, Virginia, Alabama, North Carolina, South Carolina, Delaware and Arkansas.
The company is issuing the recall to ensure that consumers are made aware of the potential hazard. No reports have been received to date of any consumer injuries or complaints.
No other sizes, varieties or other packaging configurations of SKIPPY® brand peanut butter or peanut spreads are included in this recall.
If a consumer has this product, they should return it to the store where purchased for an exchange or call Hormel Foods Customer Relations at 1-866-475-4779, Monday-Friday, 8 a.m. - 4 p.m. Central Time, excluding holidays.
This recall is being initiated out of an abundance of caution and with the knowledge of the US Food and Drug Administration.
Consumers: Hormel Foods Customer Relations: 1-866-475-4779
Hormel Foods Sales LLC is voluntarily recalling 153 cases, or 1,871 total pounds, of a single code date of SKIPPY® Reduced Fat Creamy Peanut Butter Spread, due to the possibility that some jars may contain small pieces of metal shavings which were discovered on an in-line magnet check during routine cleaning. Foodborne objects that are greater than 7mm in length may cause injury such as severe choking with airway obstruction, gastrointestinal peroration or secondary infection. The recalled product is limited to 16.3 ounce jars with a "Best If Used By" date of DEC1416LR1 with a package UPC code of 37600-10500. The code date is located on top of the lid. A photo of the product and "Best If Used By" date appears below. Recalled product was sent to distribution centers for Publix, Target and Walmart located in Georgia, Virginia, Alabama, North Carolina, South Carolina, Delaware and Arkansas.
The company is issuing the recall to ensure that consumers are made aware of the potential hazard. No reports have been received to date of any consumer injuries or complaints.
No other sizes, varieties or other packaging configurations of SKIPPY® brand peanut butter or peanut spreads are included in this recall.
If a consumer has this product, they should return it to the store where purchased for an exchange or call Hormel Foods Customer Relations at 1-866-475-4779, Monday-Friday, 8 a.m. - 4 p.m. Central Time, excluding holidays.
This recall is being initiated out of an abundance of caution and with the knowledge of the US Food and Drug Administration.
New #medical #device #recall of Quest Medical, Inc. MPS® Delivery Set due to possible seal failure.
Quest Medical, Inc. Issues Recall of MPS® Delivery Set
Consumers: custserv@questmedical.com
1-800-627-0226
On October 28, 2015, Quest Medical, Inc. initiated a nationwide recall of Myocardial Protection System (MPS) Delivery Sets, Models 5001102, 5001102-AS, and 7001102 of specified lots. The product(s) have been found to intermittently exhibit a seal failure during use, which potentially could result in patient blood loss.
There are no other recalls related to this product.
Consumers who have the applicable lots of the MPS Delivery Set(s) should cease use of the affected lots and contact Quest Medical, Inc. to return the product and request replacement. Additionally, consignees are being notified via written correspondence.
Recalled Product(s) were manufactured from May 2015 to September 2015 and distributed from June 2015 to September 2015.
The following models/UDI/ID numbers are subject to the recall:
MPS® Delivery Sets – Recall
Device Name MPS Delivery Set w/arrest agent and additive cassettes, heat exchanger & 10 ft. delivery tubing MPS Delivery Set with 6 ft. delivery tubing MPS Low Volume Delivery Set
Device Model 5001102 5001102-AS 7001102
UDI 00634624501126 00634624521124 00634624701120
Affected Lots 0491795E04, 0492175E04, 0492185E06, 0492195E06, 0492615E06, 0492625E08 0492635E08, 0489905Y04, 0490245Y06, 0493075U02, 0493085U02, 0493435U04 0493675U04, 0493685U07, 0494465U07, 0494475U09, 0494855G01, 0495215U11 0495225U11, 0495505G02, 0495515G02, 0496535G08, 0496875G08, 0496885G08 0497245S02 0492205E03 0493695U04 0494485U07 0495525G02 0497265S02 0492765E07
The affected product lot information can be identified by product labeling on shipper and individual sterile trays.
Quest Medical, Inc. voluntarily recalled the applicable lots of MPS Delivery Sets after becoming aware of complaints alleging patient blood loss from the device during use. Quest Medical, Inc. has notified the FDA of this action.
The identified lots of MPS Delivery sets have shown a possible seal failure along the blood source channel of main pump cassette, resulting in blood loss from the bypass circuit and interruption of cardioplegia solution delivery. The firm has received twenty (20) complaints alleging this seal failure which have resulted in 16 instances of patient blood loss during surgery. There have been no reports of patient injuries as a result of the alleged issue to date. The firm has reported these events via the FDA MEDWATCH program.
Quest Medical, Inc. is notifying its distributors and customers by certified letter/return receipt and is arranging for return and replacement of all recalled product(s).
Consumers with questions may contact the company via telephone at 1-800-627-0226 Monday through Friday between the hours of 9am and 5pm (CT). Consumer may also contact the company via e-mail at custserv@questmedical.com.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report Online: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
Consumers: custserv@questmedical.com
1-800-627-0226
On October 28, 2015, Quest Medical, Inc. initiated a nationwide recall of Myocardial Protection System (MPS) Delivery Sets, Models 5001102, 5001102-AS, and 7001102 of specified lots. The product(s) have been found to intermittently exhibit a seal failure during use, which potentially could result in patient blood loss.
There are no other recalls related to this product.
Consumers who have the applicable lots of the MPS Delivery Set(s) should cease use of the affected lots and contact Quest Medical, Inc. to return the product and request replacement. Additionally, consignees are being notified via written correspondence.
Recalled Product(s) were manufactured from May 2015 to September 2015 and distributed from June 2015 to September 2015.
The following models/UDI/ID numbers are subject to the recall:
MPS® Delivery Sets – Recall
Device Name MPS Delivery Set w/arrest agent and additive cassettes, heat exchanger & 10 ft. delivery tubing MPS Delivery Set with 6 ft. delivery tubing MPS Low Volume Delivery Set
Device Model 5001102 5001102-AS 7001102
UDI 00634624501126 00634624521124 00634624701120
Affected Lots 0491795E04, 0492175E04, 0492185E06, 0492195E06, 0492615E06, 0492625E08 0492635E08, 0489905Y04, 0490245Y06, 0493075U02, 0493085U02, 0493435U04 0493675U04, 0493685U07, 0494465U07, 0494475U09, 0494855G01, 0495215U11 0495225U11, 0495505G02, 0495515G02, 0496535G08, 0496875G08, 0496885G08 0497245S02 0492205E03 0493695U04 0494485U07 0495525G02 0497265S02 0492765E07
The affected product lot information can be identified by product labeling on shipper and individual sterile trays.
Quest Medical, Inc. voluntarily recalled the applicable lots of MPS Delivery Sets after becoming aware of complaints alleging patient blood loss from the device during use. Quest Medical, Inc. has notified the FDA of this action.
The identified lots of MPS Delivery sets have shown a possible seal failure along the blood source channel of main pump cassette, resulting in blood loss from the bypass circuit and interruption of cardioplegia solution delivery. The firm has received twenty (20) complaints alleging this seal failure which have resulted in 16 instances of patient blood loss during surgery. There have been no reports of patient injuries as a result of the alleged issue to date. The firm has reported these events via the FDA MEDWATCH program.
Quest Medical, Inc. is notifying its distributors and customers by certified letter/return receipt and is arranging for return and replacement of all recalled product(s).
Consumers with questions may contact the company via telephone at 1-800-627-0226 Monday through Friday between the hours of 9am and 5pm (CT). Consumer may also contact the company via e-mail at custserv@questmedical.com.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report Online: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
New pharmaceutical #drug #recall of Auvi-Q® Due to Potential Inaccurate Dosage Delivery
Sanofi US Issues Voluntary Nationwide Recall of Auvi-Q® Due to Potential Inaccurate Dosage Delivery
Consumers: Sanofi US. 1-800-981-2491
Bridgewater, N.J. - Sanofi US is voluntarily recalling all Auvi-Q® (epinephrine injection, USP). The recall involves all Auvi-Q currently on the market and includes both the 0.15 mg and 0.3 mg strengths for hospitals, retailers and consumers. This includes lot number 2299596 through 3037230, which expire March 2016 through December 2016. The products have been found to potentially have inaccurate dosage delivery.
If a patient experiencing a serious allergic reaction (i.e., anaphylaxis) did not receive the intended dose, there could be significant health consequences, including death because anaphylaxis is a potentially life-threatening condition. As of October 26, 2015, Sanofi has received 26 reports of suspected device malfunctions in the US and Canada. None of these device malfunction reports have been confirmed. In these reports, patients have described symptoms of the underlying hypersensitivity reaction. No fatal outcomes have been reported among these cases.
Auvi-Q (epinephrine injection, USP) is used to treat life-threatening allergic reactions (anaphylaxis) in people who are at risk for or have a history of these reactions. Auvi-Q is packaged with two active devices and one trainer device in a corrugate box. Auvi-Q was distributed throughout the United States via wholesalers, pharmacies and hospitals. All Auvi-Q is being recalled.
Sanofi US is notifying its distributors and customers who include doctors, pharmacies, wholesalers and other customers in the supply chain by letter, fax, email and phone calls and is arranging for return and reimbursement of all recalled products.
Customers with questions regarding this recall can go to www.Auvi-Q.com and call 1-866-726-6340 Monday through Friday 8 a.m. to 8 p.m. ET for information about how to return their Auvi-Q devices. Customers may also email cs@sanofi.com. Sanofi US will provide reimbursement for out of pocket costs incurred for the purchase of new epinephrine auto-injectors with proof of purchase.
Customers should immediately contact their healthcare provider (HCP) for a prescription for an alternate epinephrine auto-injector. In the event of a life-threatening allergic reaction (anaphylaxis), patients should only use their Auvi-Q device if another epinephrine auto-injector is not available, and then call 911 or local medical emergency services. Customers should contact their physician or HCP if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report Online: http://www.fda.gov/medwatch/report.htmdisclaimer icon
Regular Mail or Fax: Download form http://www.fda.gov/MedWatch/getforms.htmdisclaimer icon or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Sanofi US is committed to patient safety and the quality of Auvi-Q, and will continue to work closely with customers and regulatory authorities to resolve this issue in a timely manner.
Important Safety Information
Auvi-Q is for immediate self (or caregiver) administration and does not take the place of emergency medical care. Seek immediate medical treatment after use. Each Auvi-Q contains a single dose of epinephrine. Auvi-Q should only be injected into your outer thigh. DO NOT INJECT INTO BUTTOCK OR INTRAVENOUSLY. If you accidentally inject Auvi-Q into any other part of your body, seek immediate medical treatment. Epinephrine should be used with caution if you have heart disease or are taking certain medicines that can cause heart-related (cardiac) symptoms.
If you take certain medicines, you may develop serious life-threatening side effects from epinephrine. Be sure to tell your doctor about all the medicines you take, especially medicines for asthma. Side effects may be increased in patients with certain medical conditions, or who take certain medicines. These include asthma, allergies, depression, thyroid disease, Parkinson’s disease, diabetes, high blood pressure, and heart disease.
The most common side effects may include increase in heart rate, stronger or irregular heartbeat, sweating, nausea and vomiting, difficulty breathing, paleness, dizziness, weakness or shakiness, headache, apprehension, nervousness, or anxiety. These side effects go away quickly, especially if you rest.
You are encouraged to report negative side effects of prescription drugs. In the US, contact the FDA by visiting www.fda.gov/medwatch disclaimer iconor call 1-800-FDA-1088.
Please click here for Full Prescribing Information.
About Sanofi US
Sanofi, an integrated global healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients’ needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new Genzyme. Sanofi is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY).
Sanofi is the holding company of a consolidated group of subsidiaries and operates in the United States as Sanofi US. For more information on Sanofi US, please visit http://www.sanofi.us and http://www.news.sanofi.us/social-media or call 1-800-981-2491.
Forward-Looking Statements
This press release contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. These statements include projections and estimates and their underlying assumptions, statements regarding plans, objectives, intentions and expectations with respect to future financial results, events, operations, services, product development and potential, and statements regarding future performance. Forward-looking statements are generally identified by the words "expects", "anticipates", "believes", "intends", "estimates", "plans" and similar expressions. Although Sanofi's management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include among other things, the uncertainties inherent in research and development, future clinical data and analysis, including post marketing, decisions by regulatory authorities, such as the FDA or the EMA, regarding whether and when to approve any drug, device or biological application that may be filed for any such product candidates as well as their decisions regarding labelling and other matters that could affect the availability or commercial potential of such product candidates, the absence of guarantee that the product candidates if approved will be commercially successful, the future approval and commercial success of therapeutic alternatives, the Group's ability to benefit from external growth opportunities, trends in exchange rates and prevailing interest rates, the impact of cost containment policies and subsequent changes thereto, the average number of shares outstanding as well as those discussed or identified in the public filings with the SEC and the AMF made by Sanofi, including those listed under "Risk Factors" and "Cautionary Statement Regarding Forward-Looking Statements" in Sanofi's annual report on Form 20-F for the year ended December 31, 2014. Other than as required by applicable law, Sanofi does not undertake any obligation to update or revise any forward-looking information or statements.
Consumers: Sanofi US. 1-800-981-2491
Bridgewater, N.J. - Sanofi US is voluntarily recalling all Auvi-Q® (epinephrine injection, USP). The recall involves all Auvi-Q currently on the market and includes both the 0.15 mg and 0.3 mg strengths for hospitals, retailers and consumers. This includes lot number 2299596 through 3037230, which expire March 2016 through December 2016. The products have been found to potentially have inaccurate dosage delivery.
If a patient experiencing a serious allergic reaction (i.e., anaphylaxis) did not receive the intended dose, there could be significant health consequences, including death because anaphylaxis is a potentially life-threatening condition. As of October 26, 2015, Sanofi has received 26 reports of suspected device malfunctions in the US and Canada. None of these device malfunction reports have been confirmed. In these reports, patients have described symptoms of the underlying hypersensitivity reaction. No fatal outcomes have been reported among these cases.
Auvi-Q (epinephrine injection, USP) is used to treat life-threatening allergic reactions (anaphylaxis) in people who are at risk for or have a history of these reactions. Auvi-Q is packaged with two active devices and one trainer device in a corrugate box. Auvi-Q was distributed throughout the United States via wholesalers, pharmacies and hospitals. All Auvi-Q is being recalled.
Sanofi US is notifying its distributors and customers who include doctors, pharmacies, wholesalers and other customers in the supply chain by letter, fax, email and phone calls and is arranging for return and reimbursement of all recalled products.
Customers with questions regarding this recall can go to www.Auvi-Q.com and call 1-866-726-6340 Monday through Friday 8 a.m. to 8 p.m. ET for information about how to return their Auvi-Q devices. Customers may also email cs@sanofi.com. Sanofi US will provide reimbursement for out of pocket costs incurred for the purchase of new epinephrine auto-injectors with proof of purchase.
Customers should immediately contact their healthcare provider (HCP) for a prescription for an alternate epinephrine auto-injector. In the event of a life-threatening allergic reaction (anaphylaxis), patients should only use their Auvi-Q device if another epinephrine auto-injector is not available, and then call 911 or local medical emergency services. Customers should contact their physician or HCP if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report Online: http://www.fda.gov/medwatch/report.htmdisclaimer icon
Regular Mail or Fax: Download form http://www.fda.gov/MedWatch/getforms.htmdisclaimer icon or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Sanofi US is committed to patient safety and the quality of Auvi-Q, and will continue to work closely with customers and regulatory authorities to resolve this issue in a timely manner.
Important Safety Information
Auvi-Q is for immediate self (or caregiver) administration and does not take the place of emergency medical care. Seek immediate medical treatment after use. Each Auvi-Q contains a single dose of epinephrine. Auvi-Q should only be injected into your outer thigh. DO NOT INJECT INTO BUTTOCK OR INTRAVENOUSLY. If you accidentally inject Auvi-Q into any other part of your body, seek immediate medical treatment. Epinephrine should be used with caution if you have heart disease or are taking certain medicines that can cause heart-related (cardiac) symptoms.
If you take certain medicines, you may develop serious life-threatening side effects from epinephrine. Be sure to tell your doctor about all the medicines you take, especially medicines for asthma. Side effects may be increased in patients with certain medical conditions, or who take certain medicines. These include asthma, allergies, depression, thyroid disease, Parkinson’s disease, diabetes, high blood pressure, and heart disease.
The most common side effects may include increase in heart rate, stronger or irregular heartbeat, sweating, nausea and vomiting, difficulty breathing, paleness, dizziness, weakness or shakiness, headache, apprehension, nervousness, or anxiety. These side effects go away quickly, especially if you rest.
You are encouraged to report negative side effects of prescription drugs. In the US, contact the FDA by visiting www.fda.gov/medwatch disclaimer iconor call 1-800-FDA-1088.
Please click here for Full Prescribing Information.
About Sanofi US
Sanofi, an integrated global healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients’ needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new Genzyme. Sanofi is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY).
Sanofi is the holding company of a consolidated group of subsidiaries and operates in the United States as Sanofi US. For more information on Sanofi US, please visit http://www.sanofi.us and http://www.news.sanofi.us/social-media or call 1-800-981-2491.
Forward-Looking Statements
This press release contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. These statements include projections and estimates and their underlying assumptions, statements regarding plans, objectives, intentions and expectations with respect to future financial results, events, operations, services, product development and potential, and statements regarding future performance. Forward-looking statements are generally identified by the words "expects", "anticipates", "believes", "intends", "estimates", "plans" and similar expressions. Although Sanofi's management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include among other things, the uncertainties inherent in research and development, future clinical data and analysis, including post marketing, decisions by regulatory authorities, such as the FDA or the EMA, regarding whether and when to approve any drug, device or biological application that may be filed for any such product candidates as well as their decisions regarding labelling and other matters that could affect the availability or commercial potential of such product candidates, the absence of guarantee that the product candidates if approved will be commercially successful, the future approval and commercial success of therapeutic alternatives, the Group's ability to benefit from external growth opportunities, trends in exchange rates and prevailing interest rates, the impact of cost containment policies and subsequent changes thereto, the average number of shares outstanding as well as those discussed or identified in the public filings with the SEC and the AMF made by Sanofi, including those listed under "Risk Factors" and "Cautionary Statement Regarding Forward-Looking Statements" in Sanofi's annual report on Form 20-F for the year ended December 31, 2014. Other than as required by applicable law, Sanofi does not undertake any obligation to update or revise any forward-looking information or statements.
New pharmaceutical #drug #recall due to #undeclared Active Ingredients
Premiere Sales Group Issues Voluntary Nationwide Recall of All Lots of Rhino 7 3000 and Rhino 7 Platinum 3000 Capsules due to Undeclared Active Pharmaceutical Ingredients
Consumers: 888-550-8621
Premiere Sales Group of Santa Clarita, California is voluntarily recalling the following product to the consumer level: RHINO 7 3000 capsules packaged in a bottle containing six (6) capsules UPC: 616453150126 ALL LOT NUMBERS WITHIN EXPIRY and Rhino 7 Platinum 3000 Capsules packaged in a single (1) blister packs hang card count UPC: 700729253748 ALL LOT NUMBERS WITHIN EXPIRY. Lot numbers are on the back top right of the (1) count and on the side of the (6) count bottle. FDA analysis found these products to contain undeclared desmethyl carbondenafil and dapoxetine. Desmethyl carbondenafil is a phosphodiesterase PDE-5 inhibitor which is a class of drugs used to treat male erectile dysfunction, making these products unapproved new drugs. Dapoxetine is an active ingredient not approved by the U.S. Food and Drug Administration (FDA).
Desmethyl carbondenafil may pose a threat to consumers because this PDE-5 inhibitor may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels that can be life threatening. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates.
Dapoxetine has not been approved by the FDA and therefore its safety or efficacy has not been established. Chemically, dapoxetine belongs to a class of drugs known as selective serotonin reuptake inhibitors (SSRIs) used to treat depression. Studies have shown that antidepressants increased the risk of suicidal thinking and behavior in children, adolescents, and young adults when compared to placebo. Therefore, consuming these products presents a health risk which could be life threatening.
Premiere Sales has not received a report of any adverse events associated with these products.
These products are marketed as dietary supplements for sexual enhancement and packaged in (6) count bottle and (1) count hanging card and distributed to consumers nationwide. Premiere Sales Group has discontinued sales of these products.
Premiere Sales Group has notified its customers of this voluntary recall via e-mail and phone. Consumers that purchased these products from Premiere Sales Group should stop using them immediately and can return the products to : Premiere Sales Group, 21446 Golden Triangle Rd., Santa Clarita, CA 91350
Consumers with questions regarding this recall can contact Premiere Sales Group by telephone at 888-550-8621 between (Monday through Friday 7:30am to 4:00pm Pacific Standard Time Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these products. Consumers can report adverse reactions or quality control problems to the FDA’s MedWatch Adverse Event Reporting program online, by regular mail, or by fax as follows:
Complete and submit reporting form online at http://www.fda.gov/MedWatch/report.htm; or
Mail or fax reporting form. Download form at http://www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form. Complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-1078.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Consumers: 888-550-8621
Premiere Sales Group of Santa Clarita, California is voluntarily recalling the following product to the consumer level: RHINO 7 3000 capsules packaged in a bottle containing six (6) capsules UPC: 616453150126 ALL LOT NUMBERS WITHIN EXPIRY and Rhino 7 Platinum 3000 Capsules packaged in a single (1) blister packs hang card count UPC: 700729253748 ALL LOT NUMBERS WITHIN EXPIRY. Lot numbers are on the back top right of the (1) count and on the side of the (6) count bottle. FDA analysis found these products to contain undeclared desmethyl carbondenafil and dapoxetine. Desmethyl carbondenafil is a phosphodiesterase PDE-5 inhibitor which is a class of drugs used to treat male erectile dysfunction, making these products unapproved new drugs. Dapoxetine is an active ingredient not approved by the U.S. Food and Drug Administration (FDA).
Desmethyl carbondenafil may pose a threat to consumers because this PDE-5 inhibitor may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels that can be life threatening. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates.
Dapoxetine has not been approved by the FDA and therefore its safety or efficacy has not been established. Chemically, dapoxetine belongs to a class of drugs known as selective serotonin reuptake inhibitors (SSRIs) used to treat depression. Studies have shown that antidepressants increased the risk of suicidal thinking and behavior in children, adolescents, and young adults when compared to placebo. Therefore, consuming these products presents a health risk which could be life threatening.
Premiere Sales has not received a report of any adverse events associated with these products.
These products are marketed as dietary supplements for sexual enhancement and packaged in (6) count bottle and (1) count hanging card and distributed to consumers nationwide. Premiere Sales Group has discontinued sales of these products.
Premiere Sales Group has notified its customers of this voluntary recall via e-mail and phone. Consumers that purchased these products from Premiere Sales Group should stop using them immediately and can return the products to : Premiere Sales Group, 21446 Golden Triangle Rd., Santa Clarita, CA 91350
Consumers with questions regarding this recall can contact Premiere Sales Group by telephone at 888-550-8621 between (Monday through Friday 7:30am to 4:00pm Pacific Standard Time Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these products. Consumers can report adverse reactions or quality control problems to the FDA’s MedWatch Adverse Event Reporting program online, by regular mail, or by fax as follows:
Complete and submit reporting form online at http://www.fda.gov/MedWatch/report.htm; or
Mail or fax reporting form. Download form at http://www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form. Complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-1078.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Wednesday, October 28, 2015
New #foodsafety #recall possible #botulism contamination of all Sockeye Suzy canned seafood products
Sockeye Suzy's Fish Co Issuing A Voluntary Recall On All Canned Seafood Products Because Of A Possible Health Risk
Consumers: Sockeye Suzy’s Fish Co.
suzylumley@yahoo.com
509-731-0688
Sockeye Suzy’s Fish Co. of White Swan, Washington is voluntarily recalling ALL canned catfish, salmon, sturgeon, and walleye with any codes starting with “OC”, sold under brand Sockeye Suzy Fish, because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
All products were sold to consumers from our store and distributed to retail stores and wineries in Washington. The last date of distribution of recalled products was September 2015.
The affected OC code can be found on either the bottom or on top of the can. Recalled products are packaged in metal cans with net weight of 6 oz.
Product NameBrandNet Wt.UPCFancy ChinookSockeye Suzy Fish6 oz.7 48252 67292 6Fancy Spring ChinookSockeye Suzy Fish6 oz.7 48252 67412 8Peppered & Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67282 7Peppered & Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67302 2Peppered & Smoked CohoSockeye Suzy Fish6 oz.7 48252 67212 4Peppered & Smoked SteelheadSockeye Suzy Fish6 oz.7 48252 67332 9Peppered & Smoked SockeyeSockeye Suzy Fish6 oz.7 48252 67232 2Smoked CatfishSockeye Suzy Fish6 oz.7 48252 67252 0Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67282 7Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67212 4Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67302 2Smoked CohoSockeye Suzy Fish6 oz.7 48252 67222 3Smoked Garlic ChinookSockeye Suzy Fish6 oz.7 48252 67322 0Smoked Garlic SteelheadSockeye Suzy Fish6 oz.7 48252 67362 6Smoked Jalapeno ChinookSockeye Suzy Fish6 oz.7 48252 67312 1Smoked Jalapeno Spring ChinookSockeye Suzy Fish6 oz.7 48252 67392 3Smoked Jalapeno SturgeonSockeye Suzy Fish6 oz.7 48252 67272 8Smoked Jalapeno SteelheadSockeye Suzy Fish6 oz.7 48252 67352 7Smoked SockeyeSockeye Suzy Fish6 oz.7 48252 67242 1Smoked Spring ChinookSockeye Suzy Fish6 oz.7 48252 67402 9Smoked Spring ChinookSockeye Suzy Fish6 oz.7 48252 67382 4Smoked Spring ChinookSockeye Suzy Fish6 oz.7 48252 67372 5Smoked SteelheadSockeye Suzy Fish6 oz.7 48252 67342 8Smoked SturgeonSockeye Suzy Fish6 oz.7 48252 67262 9Smoked WalleyeSockeye Suzy Fish6 oz.7 94504 39610 2
There have been no reported cases of illnesses associated with our products to date.
The recalled canned seafood products were made by Skipanon Brand Seafoods LLC and this voluntary recall was initiated after we were notified that that our products were possibly under- processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers who have purchased recalled canned seafood products are urged to destroy or return it to the firm for a full refund.
If you have any questions, please call Sockeye Suzy’s Fish Co. at 509-731-0688 between the hours of 9 am and 4 pm PST, Monday-Friday, or send email to suzylumley@yahoo.com.
Consumers: Sockeye Suzy’s Fish Co.
suzylumley@yahoo.com
509-731-0688
Sockeye Suzy’s Fish Co. of White Swan, Washington is voluntarily recalling ALL canned catfish, salmon, sturgeon, and walleye with any codes starting with “OC”, sold under brand Sockeye Suzy Fish, because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
All products were sold to consumers from our store and distributed to retail stores and wineries in Washington. The last date of distribution of recalled products was September 2015.
The affected OC code can be found on either the bottom or on top of the can. Recalled products are packaged in metal cans with net weight of 6 oz.
Product NameBrandNet Wt.UPCFancy ChinookSockeye Suzy Fish6 oz.7 48252 67292 6Fancy Spring ChinookSockeye Suzy Fish6 oz.7 48252 67412 8Peppered & Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67282 7Peppered & Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67302 2Peppered & Smoked CohoSockeye Suzy Fish6 oz.7 48252 67212 4Peppered & Smoked SteelheadSockeye Suzy Fish6 oz.7 48252 67332 9Peppered & Smoked SockeyeSockeye Suzy Fish6 oz.7 48252 67232 2Smoked CatfishSockeye Suzy Fish6 oz.7 48252 67252 0Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67282 7Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67212 4Smoked ChinookSockeye Suzy Fish6 oz.7 48252 67302 2Smoked CohoSockeye Suzy Fish6 oz.7 48252 67222 3Smoked Garlic ChinookSockeye Suzy Fish6 oz.7 48252 67322 0Smoked Garlic SteelheadSockeye Suzy Fish6 oz.7 48252 67362 6Smoked Jalapeno ChinookSockeye Suzy Fish6 oz.7 48252 67312 1Smoked Jalapeno Spring ChinookSockeye Suzy Fish6 oz.7 48252 67392 3Smoked Jalapeno SturgeonSockeye Suzy Fish6 oz.7 48252 67272 8Smoked Jalapeno SteelheadSockeye Suzy Fish6 oz.7 48252 67352 7Smoked SockeyeSockeye Suzy Fish6 oz.7 48252 67242 1Smoked Spring ChinookSockeye Suzy Fish6 oz.7 48252 67402 9Smoked Spring ChinookSockeye Suzy Fish6 oz.7 48252 67382 4Smoked Spring ChinookSockeye Suzy Fish6 oz.7 48252 67372 5Smoked SteelheadSockeye Suzy Fish6 oz.7 48252 67342 8Smoked SturgeonSockeye Suzy Fish6 oz.7 48252 67262 9Smoked WalleyeSockeye Suzy Fish6 oz.7 94504 39610 2
There have been no reported cases of illnesses associated with our products to date.
The recalled canned seafood products were made by Skipanon Brand Seafoods LLC and this voluntary recall was initiated after we were notified that that our products were possibly under- processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers who have purchased recalled canned seafood products are urged to destroy or return it to the firm for a full refund.
If you have any questions, please call Sockeye Suzy’s Fish Co. at 509-731-0688 between the hours of 9 am and 4 pm PST, Monday-Friday, or send email to suzylumley@yahoo.com.
New #foodsafety #recall of sour cream & onion potato chips incorrectly labeled as gluten free
Herr's Announces Voluntary Recall of Select Bags of 1.875 oz. Sour Cream and Onion Potato Chips with Packaging Error
Consumers: 800-523-5030
Herr Foods Inc. has initiated a voluntary recall of certain bags of its 1.875 oz. Sour Cream and Onion Potato Chip due to a packaging error that incorrectly states that the product is gluten free.
While the back panel of the package complies with U.S. Food & Drug Administration (FDA) label regulations by listing “Wheat” in the ingredient statement as well as “Contains Wheat” in its related allergen statement, the front panel of the package erroneously features the words “Gluten Free.” Gluten is the protein that naturally occurs in wheat, rye, barley, and crossbreeds of these grains. Most people can eat gluten, but in people with celiac disease, gluten intake gradually damages the intestines, prevents the absorption of vitamins and minerals, and can lead to other health problems. Symptoms can include diarrhea, fatigue, headaches, abdominal pain, brain fog, rashes, nausea, vomiting, and other reactions. Herr’s has not received any reported illnesses to date.
Herr’s Sour Cream & Onion Potato Chips, 1.875 oz. bags only, were distributed nationwide through retail stores, distributors, and internet sales. These products were sold as individual bags. No other bag sizes of Herr’s Sour Cream ‘N Onion Chips are involved with this recall. No other Herr’s products are involved with this recall.
RECALLED PRODUCT
Product Name/DescriptionCode DateUPC No.Herr’s Product Code1.875 oz. Herr’s Sour Cream & Onion Potato ChipsJanuary 02, 2016, up to and including January 30, 201672600 00061122
The packages are a green metallic color bag with a red Herr’s logo at the top center of the package. The lot number is located at the upper right hand corner on the front of the package below the statement “Guaranteed Fresh Until”. The UPC number is located at the lower right hand corner of the back panel of the package.
Herr Foods announced the recall to prevent consumers who are allergic or sensitive to gluten from consuming this product. Consumers with wheat allergies, celiac disease or gluten intolerance should not consume them and should return them to the retailer where they were purchased for a full refund. Herr Foods and other retailers are removing recalled product from the retailers’ shelves. As a result, consumers can be assured that all other Herr’s products that remain on-shelf are safe and not subject to this recall. Consumers with questions may call 1-800-523-5030. Live assistance is available 9am- 5pm EST, Monday thru Friday.
Consumers: 800-523-5030
Herr Foods Inc. has initiated a voluntary recall of certain bags of its 1.875 oz. Sour Cream and Onion Potato Chip due to a packaging error that incorrectly states that the product is gluten free.
While the back panel of the package complies with U.S. Food & Drug Administration (FDA) label regulations by listing “Wheat” in the ingredient statement as well as “Contains Wheat” in its related allergen statement, the front panel of the package erroneously features the words “Gluten Free.” Gluten is the protein that naturally occurs in wheat, rye, barley, and crossbreeds of these grains. Most people can eat gluten, but in people with celiac disease, gluten intake gradually damages the intestines, prevents the absorption of vitamins and minerals, and can lead to other health problems. Symptoms can include diarrhea, fatigue, headaches, abdominal pain, brain fog, rashes, nausea, vomiting, and other reactions. Herr’s has not received any reported illnesses to date.
Herr’s Sour Cream & Onion Potato Chips, 1.875 oz. bags only, were distributed nationwide through retail stores, distributors, and internet sales. These products were sold as individual bags. No other bag sizes of Herr’s Sour Cream ‘N Onion Chips are involved with this recall. No other Herr’s products are involved with this recall.
RECALLED PRODUCT
Product Name/DescriptionCode DateUPC No.Herr’s Product Code1.875 oz. Herr’s Sour Cream & Onion Potato ChipsJanuary 02, 2016, up to and including January 30, 201672600 00061122
The packages are a green metallic color bag with a red Herr’s logo at the top center of the package. The lot number is located at the upper right hand corner on the front of the package below the statement “Guaranteed Fresh Until”. The UPC number is located at the lower right hand corner of the back panel of the package.
Herr Foods announced the recall to prevent consumers who are allergic or sensitive to gluten from consuming this product. Consumers with wheat allergies, celiac disease or gluten intolerance should not consume them and should return them to the retailer where they were purchased for a full refund. Herr Foods and other retailers are removing recalled product from the retailers’ shelves. As a result, consumers can be assured that all other Herr’s products that remain on-shelf are safe and not subject to this recall. Consumers with questions may call 1-800-523-5030. Live assistance is available 9am- 5pm EST, Monday thru Friday.
New #foodsafety #recall possible #botulism contamination of 64 oz. Canned Wild Albacore Tuna.
CSFPDX Of Garibaldi, Oregon Is Issuing A Voluntary Recall On All 64 oz. (4Lbs.) Canned Wild Albacore Tuna Because Of A Possible Health Risk
Contact: ConsumersCSFPDX
503-609-0071
CSFPDX LLC of Garibaldi, Oregon is voluntarily recalling ALL CS Fishery Wild Albacore Tuna with any codes starting with “OC”, canned by a third party, Skipanon Brand Seafoods LLC, because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
This recall only affects the CS Fishery Wild Albacore Tuna in cans, net weight 64 oz. (4 lbs.), code OCK 16APR2017 (can be found on either the bottom or on top of the can),which we purchased from Skipanon Brand Seafoods LLC. Our other canned seafood products, including 7.5 oz. canned premium Wild Line Caught Albacore Tuna, are not affected by this recall.
The recalled product was sold to consumers at our retail location or distributed to retail stores and wholesalers in Oregon. The last date of distribution of recalled products was September 2015.
There have been no reported cases of illnesses associated with our product to date.
Consumers who have purchased recalled CS Fishery Wild Albacore Tuna, 64 oz. cans, are urged to destroy or return it to the firm for a full refund.
If you have any questions, please call CSFPDX at 503-609-0071 between the hours of 9 am and 4 pm PST, Monday-Friday.
Contact: ConsumersCSFPDX
503-609-0071
CSFPDX LLC of Garibaldi, Oregon is voluntarily recalling ALL CS Fishery Wild Albacore Tuna with any codes starting with “OC”, canned by a third party, Skipanon Brand Seafoods LLC, because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
This recall only affects the CS Fishery Wild Albacore Tuna in cans, net weight 64 oz. (4 lbs.), code OCK 16APR2017 (can be found on either the bottom or on top of the can),which we purchased from Skipanon Brand Seafoods LLC. Our other canned seafood products, including 7.5 oz. canned premium Wild Line Caught Albacore Tuna, are not affected by this recall.
The recalled product was sold to consumers at our retail location or distributed to retail stores and wholesalers in Oregon. The last date of distribution of recalled products was September 2015.
There have been no reported cases of illnesses associated with our product to date.
Consumers who have purchased recalled CS Fishery Wild Albacore Tuna, 64 oz. cans, are urged to destroy or return it to the firm for a full refund.
If you have any questions, please call CSFPDX at 503-609-0071 between the hours of 9 am and 4 pm PST, Monday-Friday.
New #foodsafety #recall undeclared #allergen of egg and soy in Helados ice cream products
Helados La Tapatia, Inc. Recalls Products Because of Possible Allergens
Consumers: helatapatia@sbcqlobal.net
(559) 441-1105
Monday - Friday, 6:00 a.m. - 5:00 p.m. (PDT)
Saturday, 9:00 a.m. - 5:00 p.m. (PDT)
Helados La Tapatia, Inc., of Fresno, California, is voluntarily recalling 13 milk based ice cream products manufactured during the limited time frame of October 8, 2015, through October 16, 2015, (see separate UPC Inventory list provided herewith for detailed description) due to the inclusion of egg and soy ingredients which were not identified on product packaging and which are potential allergens to some people. The products were distributed to select retail stores in a limited area of Northern California. The products are sold under the brand name of Helados La Tapatia.
Helados La Tapatia is also voluntarily recalling its 4oz Cookies "n" Cream bar due to the undeclared Wheat and Soy and the 4oz Granola bar due to undeclared Almonds and Soy. These products were distributed in Arizona, California, Nevada, and Washington. The products are sold under the brand name of Helados La Tapatia.
People who have an allergy or severe sensitivity to soy, eggs and almonds run the risk of a serious life-threatening allergic reaction if they consume these products.
No illnesses or adverse reactions have been reported to date. The recall was the result of a routine inspection program by the U.S. FDA.
A separate UPC Inventory of the products and their UPC codes is provided.
The production and distribution of the identified products have been suspended until accurate labeling for the products is achieved. Consumers who have purchased the Helados La Tapatia products are urged to return the products to the place of purchase for a full refund.
Consumers with questions may contact the company at 1-559-441-1105 Monday through Friday, 6:00a.m. - 5:00p.m. (PDT); Saturday, 9:00a.m. - 5:00p.m. (PDT). Consumers can also contact the company athelatapatia@sbcqlobal.net.
3oz Milk BarProductUPC CodesStrawberry N Cream6 34242 20001 2Coconut6 34242 20002 9Chocolate6 34242 20003 6Banana6 34242 20004 3Vanilla6 34242 20005 0Cookies N Cream6 34242 20010 4Esquimal6 34242 20012 8Coffee6 34242 20013 5Pina Colada6 34242 20014 2Pecan6 34242 20007 4Rice6 34242 20008 1
4oz Milk BarProductUPC CodesCookies N Cream6 34242 60007 2Granola6 34242 60012 6
###
Consumers: helatapatia@sbcqlobal.net
(559) 441-1105
Monday - Friday, 6:00 a.m. - 5:00 p.m. (PDT)
Saturday, 9:00 a.m. - 5:00 p.m. (PDT)
Helados La Tapatia, Inc., of Fresno, California, is voluntarily recalling 13 milk based ice cream products manufactured during the limited time frame of October 8, 2015, through October 16, 2015, (see separate UPC Inventory list provided herewith for detailed description) due to the inclusion of egg and soy ingredients which were not identified on product packaging and which are potential allergens to some people. The products were distributed to select retail stores in a limited area of Northern California. The products are sold under the brand name of Helados La Tapatia.
Helados La Tapatia is also voluntarily recalling its 4oz Cookies "n" Cream bar due to the undeclared Wheat and Soy and the 4oz Granola bar due to undeclared Almonds and Soy. These products were distributed in Arizona, California, Nevada, and Washington. The products are sold under the brand name of Helados La Tapatia.
People who have an allergy or severe sensitivity to soy, eggs and almonds run the risk of a serious life-threatening allergic reaction if they consume these products.
No illnesses or adverse reactions have been reported to date. The recall was the result of a routine inspection program by the U.S. FDA.
A separate UPC Inventory of the products and their UPC codes is provided.
The production and distribution of the identified products have been suspended until accurate labeling for the products is achieved. Consumers who have purchased the Helados La Tapatia products are urged to return the products to the place of purchase for a full refund.
Consumers with questions may contact the company at 1-559-441-1105 Monday through Friday, 6:00a.m. - 5:00p.m. (PDT); Saturday, 9:00a.m. - 5:00p.m. (PDT). Consumers can also contact the company athelatapatia@sbcqlobal.net.
3oz Milk BarProductUPC CodesStrawberry N Cream6 34242 20001 2Coconut6 34242 20002 9Chocolate6 34242 20003 6Banana6 34242 20004 3Vanilla6 34242 20005 0Cookies N Cream6 34242 20010 4Esquimal6 34242 20012 8Coffee6 34242 20013 5Pina Colada6 34242 20014 2Pecan6 34242 20007 4Rice6 34242 20008 1
4oz Milk BarProductUPC CodesCookies N Cream6 34242 60007 2Granola6 34242 60012 6
###
Newly expanded #foodsafety #recall possible #botulism contamination of OleBob's Seafoods Canned Seafood
OleBob's Seafoods Canned Seafood Recall
Consumers: seafood@olebobs.com
(360) 642-4332
OleBob's Seafoods of Ilwaco WA is voluntarily recalling ALL canned tuna and canned salmon products with a code starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
** There have been no reported cases of illness to date. **
All products were sold under the OleBob's Seafoods label to consumers from our retail store in Ilwaco, WA, and sold to internet consumers from the websitewww.olebobs.com. The dates of distribution of recalled products were May 2014-September 2015. Affected cans have the letters "OC" stamped on either the bottom or the top of the can.
OleBob's canned salmon and tuna products were made by Skipanon Brand Seafoods and this voluntary recall was initiated after we were notified that our products were possibly under-processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers are advised to discard or return recalled product to OleBob's Seafoods for a refund.
OleBob's Seafoods
360-642-4332, 10am-5pm Thursday-Monday
seafood@olebobs.com
Consumers: seafood@olebobs.com
(360) 642-4332
OleBob's Seafoods of Ilwaco WA is voluntarily recalling ALL canned tuna and canned salmon products with a code starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
** There have been no reported cases of illness to date. **
All products were sold under the OleBob's Seafoods label to consumers from our retail store in Ilwaco, WA, and sold to internet consumers from the websitewww.olebobs.com. The dates of distribution of recalled products were May 2014-September 2015. Affected cans have the letters "OC" stamped on either the bottom or the top of the can.
OleBob's canned salmon and tuna products were made by Skipanon Brand Seafoods and this voluntary recall was initiated after we were notified that our products were possibly under-processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers are advised to discard or return recalled product to OleBob's Seafoods for a refund.
OleBob's Seafoods
360-642-4332, 10am-5pm Thursday-Monday
seafood@olebobs.com
Newly expanded #foodsafety #recall possible #botulism contamination of Gilmore Canned Sturgeon And Salmon Products
Gilmore Fish Smokehouse Is Issuing A Voluntary Recall On All Canned Sturgeon And Salmon Products Because Of A Possible Health Risk
Consumers: Gilmore Fish Smokehouse
gilmorefish@gmail.com
(509) 767-1650
Gilmore Fish of Dallesport, Washington is voluntarily recalling ALL canned (Gourmet smoked Columbia sturgeon, fresh packed Pacific salmon, gourmet smoked Chinook salmon), Gilmore Fish brand, with any codes starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
There have been no reported cases of illness to date.
All products were sold to consumers from our retail store in Dallesport, Washington. The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with "OC". The code can be found on either at the bottom or on top of the can. Recalled products are packaged in metal cans with net weight 5 oz. or 7 oz. cans.
Product NameNet WeightUPCGourmet Smoked Columbia Sturgeon5 oz.noneSmoked Wine Maple Salmon5 oz.noneSmoked Chinook Salmon7 oz.none
This voluntary recall was initiated after we were notified that our products were possibly under-processed by our contract manufacturer. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers are advised to destroy or return recalled product to Gilmore Fish Smokehouse for a refund.
If you have any questions, please contact Gilmore Fish Smokehouse at 509-767-1650 between 10am and 6pm PST, Monday-Friday or by email to gilmorefish@gmail.com.
Consumers: Gilmore Fish Smokehouse
gilmorefish@gmail.com
(509) 767-1650
Gilmore Fish of Dallesport, Washington is voluntarily recalling ALL canned (Gourmet smoked Columbia sturgeon, fresh packed Pacific salmon, gourmet smoked Chinook salmon), Gilmore Fish brand, with any codes starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
There have been no reported cases of illness to date.
All products were sold to consumers from our retail store in Dallesport, Washington. The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with "OC". The code can be found on either at the bottom or on top of the can. Recalled products are packaged in metal cans with net weight 5 oz. or 7 oz. cans.
Product NameNet WeightUPCGourmet Smoked Columbia Sturgeon5 oz.noneSmoked Wine Maple Salmon5 oz.noneSmoked Chinook Salmon7 oz.none
This voluntary recall was initiated after we were notified that our products were possibly under-processed by our contract manufacturer. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers are advised to destroy or return recalled product to Gilmore Fish Smokehouse for a refund.
If you have any questions, please contact Gilmore Fish Smokehouse at 509-767-1650 between 10am and 6pm PST, Monday-Friday or by email to gilmorefish@gmail.com.
Monday, October 26, 2015
Updated #foodsafety #recall being aided by #Josephson's Smokehouse of Skipanon Brand Seafood with possible #botulism Contamination.
Josephson's Smokehouse Aids In Seafood Recall
Consumers: Josephson's Smokehouse (503) 325-2190
Josephson's Smokehouse of Astoria, Oregon is voluntarily recalling nine canned seafood products (salmon, sturgeon and tuna) it received from Skipanon Brand Seafood of Warrenton, Oregon with any codes starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death, the U.S. Food and Drug Administration announced. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
The Josephson recall is affected by a voluntary recall initiated by Skipanon Brand Seafoods LLC following an FDA inspection that turned up a lack of documentation and potentially under-processed products.
All products were sold by Josephson's to consumers from our one retail store located in Astoria and to mail order customers through our webstore (www.josephsons.comdisclaimer icon) and telephone orders.
All mail order sales were to individual customers and were not for resale. Josephson's through their in-house invoicing and Yahoo shopping webstore invoicing system has identified all recipients of the recalled products. These recipients are being contacted by email, telephone and mail with the recall information. In addition the recall information is published on our website and is displayed in placards in our retail store.
The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with "OC". The code can be found on either the bottom or on top of the can. Recalled products are packaged in metal cans with net weight 5.5 oz., 7.0 oz., and 7.5 oz.
Product Name Net Weight UPC
Smoked Garlic Pepper Salmon 5.5 oz. (156g) 6 49586 36165 7
Smoked Wine Maple Salmon 5.5 oz. (156g) 6 49586 36160 2
Smoked Chinook Salmon 7.0 oz. (199g) 6 49586 36100 8
Premium Chinook Salmon 7.5 oz. (213g) 6 49586 36180 0
Smoked Coho Salmon 7.0 oz. (199g) 6 49586 36200 5
Fancy Coho Salmon 7.5 oz. (213g) 6 49586 36250 0
Smoked Albacore Tuna 7.0 oz. (199g) 6 49586 36600 3
Fancy Albacore Tuna 7.5 oz. (213g) 6 49586 36650 8
Smoked Sturgeon 7.0 oz. (199g) 6 49586 36500 6
There have been no reported cases of illnesses associated with our products to date.
Josephson's will replace returned cans with products that have been produced at a different processor location. The recalled cans for replacement can be brought to the retail store or mailed to Josephson's Smokehouse; 106 Marine Drive; Astoria, Oregon 97103.
Consumers who have purchased recalled canned seafood products are urged to destroy or return it to the firm for a replacement. If you have any questions, please call Josephson's Smokehouse at (503) 325-2190 between the hours of 9 am and 2 pm PST, Monday-Friday.
Consumers: Josephson's Smokehouse (503) 325-2190
Josephson's Smokehouse of Astoria, Oregon is voluntarily recalling nine canned seafood products (salmon, sturgeon and tuna) it received from Skipanon Brand Seafood of Warrenton, Oregon with any codes starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death, the U.S. Food and Drug Administration announced. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
The Josephson recall is affected by a voluntary recall initiated by Skipanon Brand Seafoods LLC following an FDA inspection that turned up a lack of documentation and potentially under-processed products.
All products were sold by Josephson's to consumers from our one retail store located in Astoria and to mail order customers through our webstore (www.josephsons.comdisclaimer icon) and telephone orders.
All mail order sales were to individual customers and were not for resale. Josephson's through their in-house invoicing and Yahoo shopping webstore invoicing system has identified all recipients of the recalled products. These recipients are being contacted by email, telephone and mail with the recall information. In addition the recall information is published on our website and is displayed in placards in our retail store.
The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with "OC". The code can be found on either the bottom or on top of the can. Recalled products are packaged in metal cans with net weight 5.5 oz., 7.0 oz., and 7.5 oz.
Product Name Net Weight UPC
Smoked Garlic Pepper Salmon 5.5 oz. (156g) 6 49586 36165 7
Smoked Wine Maple Salmon 5.5 oz. (156g) 6 49586 36160 2
Smoked Chinook Salmon 7.0 oz. (199g) 6 49586 36100 8
Premium Chinook Salmon 7.5 oz. (213g) 6 49586 36180 0
Smoked Coho Salmon 7.0 oz. (199g) 6 49586 36200 5
Fancy Coho Salmon 7.5 oz. (213g) 6 49586 36250 0
Smoked Albacore Tuna 7.0 oz. (199g) 6 49586 36600 3
Fancy Albacore Tuna 7.5 oz. (213g) 6 49586 36650 8
Smoked Sturgeon 7.0 oz. (199g) 6 49586 36500 6
There have been no reported cases of illnesses associated with our products to date.
Josephson's will replace returned cans with products that have been produced at a different processor location. The recalled cans for replacement can be brought to the retail store or mailed to Josephson's Smokehouse; 106 Marine Drive; Astoria, Oregon 97103.
Consumers who have purchased recalled canned seafood products are urged to destroy or return it to the firm for a replacement. If you have any questions, please call Josephson's Smokehouse at (503) 325-2190 between the hours of 9 am and 2 pm PST, Monday-Friday.
New #foodsafety #recall possible #listeria #adulteration of Adolf's Meat Assorted Deli Meats
Adolf’s Meat Products Recalls Assorted Deli Meat Due to Possible Listeria Adulteration
Class I Recall 132-2015
Health Risk: High Oct 26, 2015
Julie Schwartz
(202) 720-9113
WASHINGTON, Oct. 26, 2015 – Adolf’s Meat Products, a Hartford, Conn. establishment, is recalling approximately 224 pounds of assorted meat that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The following items, produced on Oct. 20, 2015, are subject to recall: [View Label]
14-lb. of Smoked Kielbasa
100-lb. of Hams
40-lb. of Canadian Bacon
30-lb. of Bone-In Pork Loins
50-lb. of Liverwurst
The smoked kielbasa products bear establishment number “EST. 34651” inside the USDA mark of inspection, while other products were sold without labels from behind deli counters. All recalled products were sold at retail locations in Connecticut.
The problem was discovered during routine FSIS sample testing. There have been no confirmed reports of adverse reactions due to consumption of these products.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS and the company are concerned that some product may be frozen and in consumers' freezers.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
FSIS advises all consumers to reheat ready-to-eat product until steaming hot.
Media and consumers with questions regarding the recall can contact Joseph Gorski, President, at (860) 522-1588.
Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at: http://www.fsis.usda.gov/reportproblem.
Class I Recall 132-2015
Health Risk: High Oct 26, 2015
Julie Schwartz
(202) 720-9113
WASHINGTON, Oct. 26, 2015 – Adolf’s Meat Products, a Hartford, Conn. establishment, is recalling approximately 224 pounds of assorted meat that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The following items, produced on Oct. 20, 2015, are subject to recall: [View Label]
14-lb. of Smoked Kielbasa
100-lb. of Hams
40-lb. of Canadian Bacon
30-lb. of Bone-In Pork Loins
50-lb. of Liverwurst
The smoked kielbasa products bear establishment number “EST. 34651” inside the USDA mark of inspection, while other products were sold without labels from behind deli counters. All recalled products were sold at retail locations in Connecticut.
The problem was discovered during routine FSIS sample testing. There have been no confirmed reports of adverse reactions due to consumption of these products.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS and the company are concerned that some product may be frozen and in consumers' freezers.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
FSIS advises all consumers to reheat ready-to-eat product until steaming hot.
Media and consumers with questions regarding the recall can contact Joseph Gorski, President, at (860) 522-1588.
Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at: http://www.fsis.usda.gov/reportproblem.
New #foodsafety #recall undeclared #allergen of #soy in Skinny Latina Foods Million Dollar Marinade
Skinny Latina Foods, Inc. Issues Recall for Undeclared Soy
Consumers: Bibi (305) 609-3310
Skinny Latina Foods, Inc. Miami, Florida is recalling all bottles of the following product due to undeclared soy. People who have an allergy or severe sensitivity to soy run the risk of serious life threatening allergic reaction if they consume these products. No illnesses have been reported to date in connection with this recall.
The product is only sold in clear, 12 oz glass bottles. Each product is labeled with a "Best By" date on the back label. The recall is for all of the individual bottles with the "Best By" date of 12-15-15 or before (earlier), and which do not have corrected labels indicating that the product contains soy.
The recalled products were distributed in retail stores nationwide.
The recall was initiated after it was discovered that product containing soy within the gluten-free teriyaki sauce ingredient of the product was distributed in packaging that did not reveal the presence of the soy allergen on the label.
The U.S. Food and Drug Administration have been notified of this voluntary recall.
Purchasers allergic to soy and / or soybean should destroy the product, or contact Skinny Latina Foods, Inc. for more information. Anyone with questions, please contact Bibi at Skinny Latina at (305) 609-3310.
Consumers: Bibi (305) 609-3310
Skinny Latina Foods, Inc. Miami, Florida is recalling all bottles of the following product due to undeclared soy. People who have an allergy or severe sensitivity to soy run the risk of serious life threatening allergic reaction if they consume these products. No illnesses have been reported to date in connection with this recall.
The product is only sold in clear, 12 oz glass bottles. Each product is labeled with a "Best By" date on the back label. The recall is for all of the individual bottles with the "Best By" date of 12-15-15 or before (earlier), and which do not have corrected labels indicating that the product contains soy.
The recalled products were distributed in retail stores nationwide.
The recall was initiated after it was discovered that product containing soy within the gluten-free teriyaki sauce ingredient of the product was distributed in packaging that did not reveal the presence of the soy allergen on the label.
The U.S. Food and Drug Administration have been notified of this voluntary recall.
Purchasers allergic to soy and / or soybean should destroy the product, or contact Skinny Latina Foods, Inc. for more information. Anyone with questions, please contact Bibi at Skinny Latina at (305) 609-3310.
New #foodsafety #recall undeclared #allergen of #milk in certain products containing candy buttons
Kanan Enterprises Conducts Nationwide Voluntary Recall of Certain Products Containing Candy Buttons
Contact
Consumers: Consumer Help Line: 1-800-860-5464
Firm Press Release
Solon, OH - Kanan Enterprises announces the voluntary recall of multiple products that contain candy buttons due to the presence of an ingredient that contains milk protein, which is not declared on the packaging. This candy button came from an outside ingredient supplier. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume these products. Kanan Enterprises was made aware of this issue through notification by a customer that we co-pack for. Kanan Enterprises is aware of one consumer allergic reaction associated with consumption of this product..
A list of affected products and code dates is listed below:
BrandProductSizePackageDate CodeUPC CodeBetter ValuMountain Mix10 oz.Stand Up PouchAll date codes0 79801 24706 8FavoritesMountain Mix7 oz.Stand Up PouchDate codes earlier than Best Before 06Aug20160 38445 12280 3Clear ValueMountain Mix10 oz.Stand Up PouchDate codes earlier than Best By 06May160 36800 36285 7King'sMountain Trail Mix25 lbs.Bulk CaseAll date codesItem # 00440King'sMountain Mix2 oz.Pillow BagAll date codes0 38445 00224 2King'sMountain Mix28 oz.Stand Up PouchAll date codes0 38445 43431 9King'sSweet & Salty Mix25 lbs.CaseAll date codesItem #00389King'sSweet & Salty Mix16 oz.Plastic JarAll date codes0 38445 13192 8King'sSweet & Salty Mix6.5 oz.Pillow BagDate codes earlier than Best By May 21 160 38445 54309 7King'sSweet & Salty Mix5 oz.Pillow BagDate codes earlier than Best By May 21 160 38445 54309 7King'sPenguin Tin Mountain Trail Mix17 oz.TinAll date codesItem # 7463017Speedy ChoiceTrail Mix Salty & Sweet8 oz.Stand Up PouchAll date codes0 52894 12056 2Speedy ChoiceTrail Mix Salty & Sweet2.75 oz.Tube BagDate codes earlier than Best By 19 Aug 20160 52894 12062 3Valu TimeMountain Mix10 oz.Stand Up PouchAll date codes0 11225 09157King’sCashews & Sweeties14 oz.Stand Up PouchAll date codes0 38445 49999 8
Consumers with this reported product should not consume this product. They should destroy it or return it to the point of purchase. Consumers with questions should call 1-800-860-5464, 8:15 am - 5:00pm EST, Monday - Friday
Contact
Consumers: Consumer Help Line: 1-800-860-5464
Firm Press Release
Solon, OH - Kanan Enterprises announces the voluntary recall of multiple products that contain candy buttons due to the presence of an ingredient that contains milk protein, which is not declared on the packaging. This candy button came from an outside ingredient supplier. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume these products. Kanan Enterprises was made aware of this issue through notification by a customer that we co-pack for. Kanan Enterprises is aware of one consumer allergic reaction associated with consumption of this product..
A list of affected products and code dates is listed below:
BrandProductSizePackageDate CodeUPC CodeBetter ValuMountain Mix10 oz.Stand Up PouchAll date codes0 79801 24706 8FavoritesMountain Mix7 oz.Stand Up PouchDate codes earlier than Best Before 06Aug20160 38445 12280 3Clear ValueMountain Mix10 oz.Stand Up PouchDate codes earlier than Best By 06May160 36800 36285 7King'sMountain Trail Mix25 lbs.Bulk CaseAll date codesItem # 00440King'sMountain Mix2 oz.Pillow BagAll date codes0 38445 00224 2King'sMountain Mix28 oz.Stand Up PouchAll date codes0 38445 43431 9King'sSweet & Salty Mix25 lbs.CaseAll date codesItem #00389King'sSweet & Salty Mix16 oz.Plastic JarAll date codes0 38445 13192 8King'sSweet & Salty Mix6.5 oz.Pillow BagDate codes earlier than Best By May 21 160 38445 54309 7King'sSweet & Salty Mix5 oz.Pillow BagDate codes earlier than Best By May 21 160 38445 54309 7King'sPenguin Tin Mountain Trail Mix17 oz.TinAll date codesItem # 7463017Speedy ChoiceTrail Mix Salty & Sweet8 oz.Stand Up PouchAll date codes0 52894 12056 2Speedy ChoiceTrail Mix Salty & Sweet2.75 oz.Tube BagDate codes earlier than Best By 19 Aug 20160 52894 12062 3Valu TimeMountain Mix10 oz.Stand Up PouchAll date codes0 11225 09157King’sCashews & Sweeties14 oz.Stand Up PouchAll date codes0 38445 49999 8
Consumers with this reported product should not consume this product. They should destroy it or return it to the point of purchase. Consumers with questions should call 1-800-860-5464, 8:15 am - 5:00pm EST, Monday - Friday
Saturday, October 24, 2015
New #foodsafety #recall possible #listeria contamination of Whole Foods Market Curry Chicken Salad Product
Whole Foods Market Recalls Curry Chicken Salad Product Due To Possible Listeria Adulteration
Class I Recall 131-2015
Health Risk: High Oct 24, 2015
Congressional and Public Affairs: Julie Schwartz (202) 720-9113
WASHINGTON, Oct. 24, 2015 – A Whole Foods Market establishment located in Everett, Mass. is recalling approximately 234 pounds of curry chicken salad products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The chicken curry salad was packaged on Oct. 16, 2015, and was sold prepackaged, in salad bars, in store's chef's cases, and in sandwiches and wraps prepared in the stores. The following products are subject to recall: [Labels (PDF Only)]
Sold by weight “Curry Chicken Salad, Our Chef’s Own” bearing UPC Code # 285551.
Sold by weight “Curry Chicken Salad CC” bearing UPC Code # 261068.
Sold by weight “PPK Salad Chicken Curry” bearing UPC Code # 263142
12 oz. “Curry Chicken Salad Wrap, Made Right Here” bearing UPC Code # 263144.
7 oz. “Single Curry Chicken Salad Wrap, Made Right Here” bearing UPC Code # 263126.
7 oz. “Curry Chicken Salad Rollup” bearing UPC Code # 265325.
These items have a sell by date of Oct. 23, 2015 and were shipped to a warehouse and retail locations in Connecticut, Massachusetts, New Jersey, New York, and Rhode Island.
The problem was discovered when FSIS was notified of sample testing results performed by the Massachusetts Department of Public Health. There have been no confirmed reports of adverse reactions due to consumption of these products.
Consumption of food adulterated by L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating adulterated food should seek medical care and tell the health care provider about eating the adulterated food.
FSIS and the company are concerned that some product may be at home in consumers' freezers or refrigerators.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Related items, including the Whole Foods Class Deli Pasta Salad, have been listed for recall on the U.S. Food and Drug Administration’s website at http://www.fda.gov/Safety/Recalls/ucm469008.htm.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
FSIS advises all consumers to reheat ready-to-eat product until steaming hot.
Media and consumers with questions regarding the recall can contact Heather McCready, Public Relations Manager, at (617) 492-5500.
Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at: http://www.fsis.usda.gov/reportproblem.
Class I Recall 131-2015
Health Risk: High Oct 24, 2015
Congressional and Public Affairs: Julie Schwartz (202) 720-9113
WASHINGTON, Oct. 24, 2015 – A Whole Foods Market establishment located in Everett, Mass. is recalling approximately 234 pounds of curry chicken salad products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The chicken curry salad was packaged on Oct. 16, 2015, and was sold prepackaged, in salad bars, in store's chef's cases, and in sandwiches and wraps prepared in the stores. The following products are subject to recall: [Labels (PDF Only)]
Sold by weight “Curry Chicken Salad, Our Chef’s Own” bearing UPC Code # 285551.
Sold by weight “Curry Chicken Salad CC” bearing UPC Code # 261068.
Sold by weight “PPK Salad Chicken Curry” bearing UPC Code # 263142
12 oz. “Curry Chicken Salad Wrap, Made Right Here” bearing UPC Code # 263144.
7 oz. “Single Curry Chicken Salad Wrap, Made Right Here” bearing UPC Code # 263126.
7 oz. “Curry Chicken Salad Rollup” bearing UPC Code # 265325.
These items have a sell by date of Oct. 23, 2015 and were shipped to a warehouse and retail locations in Connecticut, Massachusetts, New Jersey, New York, and Rhode Island.
The problem was discovered when FSIS was notified of sample testing results performed by the Massachusetts Department of Public Health. There have been no confirmed reports of adverse reactions due to consumption of these products.
Consumption of food adulterated by L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating adulterated food should seek medical care and tell the health care provider about eating the adulterated food.
FSIS and the company are concerned that some product may be at home in consumers' freezers or refrigerators.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Related items, including the Whole Foods Class Deli Pasta Salad, have been listed for recall on the U.S. Food and Drug Administration’s website at http://www.fda.gov/Safety/Recalls/ucm469008.htm.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
FSIS advises all consumers to reheat ready-to-eat product until steaming hot.
Media and consumers with questions regarding the recall can contact Heather McCready, Public Relations Manager, at (617) 492-5500.
Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at: http://www.fsis.usda.gov/reportproblem.
New #foodsafety #recall #undeclared dairy in David Trail Mix Sweet & Salty.
David Trail Mix Sweet & Salty Voluntarily Recalled Due To Undeclared Dairy Allergen
Consumers: (800) 881-3989
DAVID® Trail Mix Sweet & Salty flavor is being voluntarily recalled by ConAgra Foods due to the presence of an ingredient in the trail mix that contains milk protein, which is not declared on the packaging.
This Smart News Release features multimedia. View the full release here:http://www.businesswire.com/news/home/20151023006019/en/
The finished product is made for ConAgra Foods by a third party supplier who is conducting a separate recall for similar, impacted products.
This food is a concern for people who are allergic to milk. People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume the product. ConAgra Foods was made aware of this issue through a consumer contact. ConAgra Foods is aware of one consumer allergic reaction associated with consumption of this product.
ConAgra Foods is advising consumers who have purchased this item to discard it or return it to the store where originally purchased. This recall includes the following DAVID Trail Mix Sweet & Salty products sold as part of multi-variety packages that also contain DAVID Trail Mix Classic. DAVID Trail Mix Classic is not impacted by this recall:
UPC 26200 23884 5oz. bags/149g
The product was shipped to retail food stores and distributors in the U.S. and Mexico. ConAgra Foods is working with retail customers and distributors to ensure the packages are removed from store shelves.
This recall is limited to DAVID Trail Mix Sweet & Salty flavor only and does not impact other flavors of DAVID Trail Mix or any DAVID Seeds products.
Consumers with questions should call our Consumer Affairs hotline at: (800) 881-3989, open 24 hours a day/7 days a week.
Consumers: (800) 881-3989
DAVID® Trail Mix Sweet & Salty flavor is being voluntarily recalled by ConAgra Foods due to the presence of an ingredient in the trail mix that contains milk protein, which is not declared on the packaging.
This Smart News Release features multimedia. View the full release here:http://www.businesswire.com/news/home/20151023006019/en/
The finished product is made for ConAgra Foods by a third party supplier who is conducting a separate recall for similar, impacted products.
This food is a concern for people who are allergic to milk. People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume the product. ConAgra Foods was made aware of this issue through a consumer contact. ConAgra Foods is aware of one consumer allergic reaction associated with consumption of this product.
ConAgra Foods is advising consumers who have purchased this item to discard it or return it to the store where originally purchased. This recall includes the following DAVID Trail Mix Sweet & Salty products sold as part of multi-variety packages that also contain DAVID Trail Mix Classic. DAVID Trail Mix Classic is not impacted by this recall:
UPC 26200 23884 5oz. bags/149g
The product was shipped to retail food stores and distributors in the U.S. and Mexico. ConAgra Foods is working with retail customers and distributors to ensure the packages are removed from store shelves.
This recall is limited to DAVID Trail Mix Sweet & Salty flavor only and does not impact other flavors of DAVID Trail Mix or any DAVID Seeds products.
Consumers with questions should call our Consumer Affairs hotline at: (800) 881-3989, open 24 hours a day/7 days a week.
New #foodsafety #recall of Ethereal Confections Chocolates due to #undeclared milk, a known #allergen
Ethereal Confections Issues Allergy Alert On Undeclared Amounts Of Milk In Chocolates
Consumers: Ethereal Confections: orders@etherealconfections.com or (815) 687-0320
Ethereal Confections of Woodstock, IL is recalling all Inclusion Bars & Mendiants with expiration dates of 10/22/2015 through 04/15/2016 and all Meltaway Bars & Meltaways with expiration dates of 10/22/2015 through 01/15/2016, because they may contain undeclared amounts of milk. People who have an allergy or severe sensitivity to milk run the risk of serious or lifethreatening allergic reaction if they consume these products.
Product was distributed by Ethereal Confections to retail stores throughout the United States, sold at Ethereal Confections in Woodstock, IL, and sold online at www.etherealconfections.com. Product was distributed from 4/22/2015 through 10/15/2015.
Here is a complete list of the affected products and their respective UPCs:
SKU UPC Description Exp Start Date Exp End Date
CB1021 857234003006 Inclusion Bar - Macadamia Nuts + Raspberries + Kaffir Lime 10/21/2015 4/15/2016
CB1022 857234003013 Inclusion Bar - Pistachios + Cranberries + Sea Salt 10/21/2015 4/15/2016
CB1023 857234003020 Inclusion Bar - Candied Ginger + Candied Orange Peel + Coriander 10/21/2015 4/15/2016
CB1024 857234003051 Inclusion Bar - Strawberries + Rose Petals + Pink Peppercorns 10/21/2015 4/15/2016
CB1025 857234003037 Inclusion Bar - Blueberries+ Cherries + Blackberries 10/21/2015 4/15/2016
CB1026 857234003068 Inclusion Bar - Cherries + Cocoa Nibs + Cayenne 10/21/2015 4/15/2016
CB1027 857234003310 Inclusion Bar - Strawberries + Mangoes + Chiles 10/21/2015 4/15/2016
CB1028 857234003327 Inclusion Bar - Espresso + Cherries + Hazelnuts 10/21/2015 4/15/2016
CB1029 857234003358 Inclusion Bar - Scorpion Pepper + Bourbon + Smoked Sea Salt + Caramel Pecans 10/21/2015 4/15/2016
CB1030 857234003334 Inclusion Bar - Cocao Nibs + Caramel Almonds + Sea Salt 10/21/2015 4/15/2016
MB1021 857234003280 Meltaway Bar - Black Cherry Lemonade 10/21/2015 1/15/2016
MB1022 857234003280 Meltaway Bar - Black Cherry Lemonade 10/21/2015 1/15/2016
MB1023 857234003273 Meltaway Bar - Blood Orange & Vanilla Bean 10/21/2015 1/15/2016
MB1024 857234003303 Meltaway Bar - French Vanilla & Salted Almond 10/21/2015 1/15/2016
MDOACH 857234003266 Mendiant - Orange, Apricot & Carmelized Hazelnut 10/21/2015 4/15/2016
MDPRC 857234003259 Mendiant - Pistachio, Rose Petal & Candied Ginger 10/21/2015 4/15/2016
ML1031 857234003112 Meltaways - 3 Piece Peppermint Meltaways 10/21/2015 1/15/2016
ML1032 857234003136 Meltaways - 3 Piece Vanilla Sea Salt Meltaways 10/21/2015 1/15/2016
ML1033 857234003105 Meltaways - 3 Piece Blood Orange Meltaways 10/21/2015 1/15/2016
ML1034 857234003082 Meltaways - Piece Tahitian Vanilla Lemon Meltaways 10/21/2015 1/15/2016
ML1035 857234003129 Meltaways - Piece Meltaways Assorted 10/21/2015 1/15/2016
No illnesses have been reported to date in connection with this problem.
The recall was initiated due to FDA testing that found the presence of milk. The product, labeled as "dairy free", contains levels of milk protein that can elicit lifethreatening reactions in milk-allergic individuals.
Consumers and wholesale customers who have purchased product from Ethereal Confections meeting the above criteria are urged to contact Ethereal Confections at 8156870320 or email orders@etherealconfections.com.
Please contact Ethereal Confections 7 days a week between the hours of 9:00am and 5:00pm, Central Time Zone.
Consumers: Ethereal Confections: orders@etherealconfections.com or (815) 687-0320
Ethereal Confections of Woodstock, IL is recalling all Inclusion Bars & Mendiants with expiration dates of 10/22/2015 through 04/15/2016 and all Meltaway Bars & Meltaways with expiration dates of 10/22/2015 through 01/15/2016, because they may contain undeclared amounts of milk. People who have an allergy or severe sensitivity to milk run the risk of serious or lifethreatening allergic reaction if they consume these products.
Product was distributed by Ethereal Confections to retail stores throughout the United States, sold at Ethereal Confections in Woodstock, IL, and sold online at www.etherealconfections.com. Product was distributed from 4/22/2015 through 10/15/2015.
Here is a complete list of the affected products and their respective UPCs:
SKU UPC Description Exp Start Date Exp End Date
CB1021 857234003006 Inclusion Bar - Macadamia Nuts + Raspberries + Kaffir Lime 10/21/2015 4/15/2016
CB1022 857234003013 Inclusion Bar - Pistachios + Cranberries + Sea Salt 10/21/2015 4/15/2016
CB1023 857234003020 Inclusion Bar - Candied Ginger + Candied Orange Peel + Coriander 10/21/2015 4/15/2016
CB1024 857234003051 Inclusion Bar - Strawberries + Rose Petals + Pink Peppercorns 10/21/2015 4/15/2016
CB1025 857234003037 Inclusion Bar - Blueberries+ Cherries + Blackberries 10/21/2015 4/15/2016
CB1026 857234003068 Inclusion Bar - Cherries + Cocoa Nibs + Cayenne 10/21/2015 4/15/2016
CB1027 857234003310 Inclusion Bar - Strawberries + Mangoes + Chiles 10/21/2015 4/15/2016
CB1028 857234003327 Inclusion Bar - Espresso + Cherries + Hazelnuts 10/21/2015 4/15/2016
CB1029 857234003358 Inclusion Bar - Scorpion Pepper + Bourbon + Smoked Sea Salt + Caramel Pecans 10/21/2015 4/15/2016
CB1030 857234003334 Inclusion Bar - Cocao Nibs + Caramel Almonds + Sea Salt 10/21/2015 4/15/2016
MB1021 857234003280 Meltaway Bar - Black Cherry Lemonade 10/21/2015 1/15/2016
MB1022 857234003280 Meltaway Bar - Black Cherry Lemonade 10/21/2015 1/15/2016
MB1023 857234003273 Meltaway Bar - Blood Orange & Vanilla Bean 10/21/2015 1/15/2016
MB1024 857234003303 Meltaway Bar - French Vanilla & Salted Almond 10/21/2015 1/15/2016
MDOACH 857234003266 Mendiant - Orange, Apricot & Carmelized Hazelnut 10/21/2015 4/15/2016
MDPRC 857234003259 Mendiant - Pistachio, Rose Petal & Candied Ginger 10/21/2015 4/15/2016
ML1031 857234003112 Meltaways - 3 Piece Peppermint Meltaways 10/21/2015 1/15/2016
ML1032 857234003136 Meltaways - 3 Piece Vanilla Sea Salt Meltaways 10/21/2015 1/15/2016
ML1033 857234003105 Meltaways - 3 Piece Blood Orange Meltaways 10/21/2015 1/15/2016
ML1034 857234003082 Meltaways - Piece Tahitian Vanilla Lemon Meltaways 10/21/2015 1/15/2016
ML1035 857234003129 Meltaways - Piece Meltaways Assorted 10/21/2015 1/15/2016
No illnesses have been reported to date in connection with this problem.
The recall was initiated due to FDA testing that found the presence of milk. The product, labeled as "dairy free", contains levels of milk protein that can elicit lifethreatening reactions in milk-allergic individuals.
Consumers and wholesale customers who have purchased product from Ethereal Confections meeting the above criteria are urged to contact Ethereal Confections at 8156870320 or email orders@etherealconfections.com.
Please contact Ethereal Confections 7 days a week between the hours of 9:00am and 5:00pm, Central Time Zone.
New #petfood #recall possible @salmonella contamination of Good N Fun Beefhide Chicken Sticks Dog Treats
Salix Animal Health, LLC, Expands Voluntary Recall of Good N Fun Beefhide Chicken Sticks Dog Treats Due To Possible Salmonella Contamination
Consumers: 1-800-338-4896
Salix Animal Health, LLC of Deerfield, FL is voluntarily expanding its recall of "Good 'n' Fun - Beefhide Chicken Sticks" because this product may be contaminated with Salmonella.
Sampling conducted by the Georgia Department of Agriculture confirmed the presence of Salmonella in an additional lot of this product. In an abundance of caution, Salix Animal Health is expanding its original recall to include the tested lot and others made around the same timeframe. This affects Good 'n' Fun - Beefhide Chicken Sticks only; no other product is affected by this announcement.
Salmonella can affect animals that eat contaminated products and there is a potential risk to humans if they come in contact with Salmonella from handling contaminated products.
Healthy people infected with Salmonella should monitor themselves for some, or all, of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.
Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected, but otherwise healthy pets can be carriers of Salmonella and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.
The recalled Good 'n' Fun - Beefhide Chicken Sticks were distributed nationwide to Dollar General, Dollar Tree and Family Dollar retail stores. The recalled product is packaged in a 2.8 ounce bag stamped on the back side with an item code number of 82247 and with an expiration date ranging from 02/2018- 07/2018.
The UPC code is 0 91093 82247 1 as shown in the table below.
Brand Size Description UPC Code Item No. Expiration
Good ‘n’ Fun 2.8 oz Beefhide Chicken Sticks 091093822471 82247 02/2018
03/2018
04/2018
05/2018
06/2018
07/2018
No other product is affected at this time. Customers should look at the item number, and expiration date on the product package to determine if it is subject to the voluntary recall. Customers who have purchased the product subject to this recall are urged to dispose of the product or return it for full refund.
We take our responsibility to pets and their owners seriously and are taking steps to prevent it from occurring in the future. Salix Animal Health is also working with retailers to ensure that the affected product is removed from inventory and is no longer sold.
If you have these products, please contact Salix Animal Health’s consumer affairs team at 1-800-338-4896, Monday through Friday between the hours of 8:30 AM – 5:00 PM Eastern Standard Time for a refund. Customers with questions may call the consumer affairs team at the number listed above.
For press inquiries, please contact Connie Caldwell at 314-683-2460, Monday through Friday 9:00 AM - 6:00 PM Eastern Standard Time.
Consumers: 1-800-338-4896
Salix Animal Health, LLC of Deerfield, FL is voluntarily expanding its recall of "Good 'n' Fun - Beefhide Chicken Sticks" because this product may be contaminated with Salmonella.
Sampling conducted by the Georgia Department of Agriculture confirmed the presence of Salmonella in an additional lot of this product. In an abundance of caution, Salix Animal Health is expanding its original recall to include the tested lot and others made around the same timeframe. This affects Good 'n' Fun - Beefhide Chicken Sticks only; no other product is affected by this announcement.
Salmonella can affect animals that eat contaminated products and there is a potential risk to humans if they come in contact with Salmonella from handling contaminated products.
Healthy people infected with Salmonella should monitor themselves for some, or all, of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.
Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected, but otherwise healthy pets can be carriers of Salmonella and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.
The recalled Good 'n' Fun - Beefhide Chicken Sticks were distributed nationwide to Dollar General, Dollar Tree and Family Dollar retail stores. The recalled product is packaged in a 2.8 ounce bag stamped on the back side with an item code number of 82247 and with an expiration date ranging from 02/2018- 07/2018.
The UPC code is 0 91093 82247 1 as shown in the table below.
Brand Size Description UPC Code Item No. Expiration
Good ‘n’ Fun 2.8 oz Beefhide Chicken Sticks 091093822471 82247 02/2018
03/2018
04/2018
05/2018
06/2018
07/2018
No other product is affected at this time. Customers should look at the item number, and expiration date on the product package to determine if it is subject to the voluntary recall. Customers who have purchased the product subject to this recall are urged to dispose of the product or return it for full refund.
We take our responsibility to pets and their owners seriously and are taking steps to prevent it from occurring in the future. Salix Animal Health is also working with retailers to ensure that the affected product is removed from inventory and is no longer sold.
If you have these products, please contact Salix Animal Health’s consumer affairs team at 1-800-338-4896, Monday through Friday between the hours of 8:30 AM – 5:00 PM Eastern Standard Time for a refund. Customers with questions may call the consumer affairs team at the number listed above.
For press inquiries, please contact Connie Caldwell at 314-683-2460, Monday through Friday 9:00 AM - 6:00 PM Eastern Standard Time.
New #foodsafety #recall possible #listeria contamination of Curry Chicken Salad and Classic Deli Pasta Salad from #wholefoods in Seven States
Whole Foods Market Recalls Curry Chicken Salad and Classic Deli Pasta Salad in Seven States Due to Possible Listeria Contamination
Consumers: 617-492-5500
Whole Foods Market of Cambridge, Massachusetts, is recalling bulk and packaged Curry Chicken Salad and Classic Deli Pasta Salad sold in stores in ME, NH, MA, RI, CT, NY and NJ because it has the potential to be contaminated with Listeria Monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. Consumers should seek immediate medical care if they develop these symptoms.
No illnesses have been reported.
The salads were sold prepackaged, in salad bars, in store's chef's cases and in sandwiches and wraps prepared in the stores. The effected products were sold in stores between October 18 and October 22, 2015 and have a "sell by" date of October 23, 2015. The recalled items include:
UPC Code Product Description Lot Code
285551 Curry Chicken Salad, Our Chef’s Own, sold by weight Sell by 10/23/15
263144 Curry Chicken Salad Wrap, Made Right Here, sold by weight, 12oz Sell by 10/23/15
263126 Single Curry Chicken Salad Wrap, Made Right Here, 7oz Sell by 10/23/15
261068 Curry Chicken Salad CC, sold by weight Sell by 10/23/15
263142 PPK Salad Chicken Curry, sold by weight Sell by 10/23/15
265325 Curry Chicken Salad Rollup, 7oz Sell by 10/23/15
260976 Classic Deli Pasta Salad, Sold by weight Sell by 10/23/15
270742 FP Pasta Salad Classic Deli, sold by weight Sell by 10/23/15
0 36406 30001 7 Classic Deli Pasta Salad, 6oz Sell by 10/23/15
0 36406 30264 6 Classic Deli Pasta Salad, 14 oz Sell by 10/23/15
A sampling of the products tested positive for Listeria Monocytogenes during a routine inspection of Whole Foods Market's North Atlantic Kitchen facility.
Consumers who have purchased this product from Whole Foods Market should discard it and bring their receipt to the store for a full refund. Consumers with questions should contact their local store or call 617-492-5500 between the hours of 9am and 5pm EST.
Consumers: 617-492-5500
Whole Foods Market of Cambridge, Massachusetts, is recalling bulk and packaged Curry Chicken Salad and Classic Deli Pasta Salad sold in stores in ME, NH, MA, RI, CT, NY and NJ because it has the potential to be contaminated with Listeria Monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. Consumers should seek immediate medical care if they develop these symptoms.
No illnesses have been reported.
The salads were sold prepackaged, in salad bars, in store's chef's cases and in sandwiches and wraps prepared in the stores. The effected products were sold in stores between October 18 and October 22, 2015 and have a "sell by" date of October 23, 2015. The recalled items include:
UPC Code Product Description Lot Code
285551 Curry Chicken Salad, Our Chef’s Own, sold by weight Sell by 10/23/15
263144 Curry Chicken Salad Wrap, Made Right Here, sold by weight, 12oz Sell by 10/23/15
263126 Single Curry Chicken Salad Wrap, Made Right Here, 7oz Sell by 10/23/15
261068 Curry Chicken Salad CC, sold by weight Sell by 10/23/15
263142 PPK Salad Chicken Curry, sold by weight Sell by 10/23/15
265325 Curry Chicken Salad Rollup, 7oz Sell by 10/23/15
260976 Classic Deli Pasta Salad, Sold by weight Sell by 10/23/15
270742 FP Pasta Salad Classic Deli, sold by weight Sell by 10/23/15
0 36406 30001 7 Classic Deli Pasta Salad, 6oz Sell by 10/23/15
0 36406 30264 6 Classic Deli Pasta Salad, 14 oz Sell by 10/23/15
A sampling of the products tested positive for Listeria Monocytogenes during a routine inspection of Whole Foods Market's North Atlantic Kitchen facility.
Consumers who have purchased this product from Whole Foods Market should discard it and bring their receipt to the store for a full refund. Consumers with questions should contact their local store or call 617-492-5500 between the hours of 9am and 5pm EST.
Friday, October 23, 2015
New #foodsafety #recall Possible #botulisim contamination of Seaquest Seafood Corp. Dehydrated & Marinated Uneviscerated Fish
Seaquest Seafood Corp. Recalling Dehydrated & Marinated Uneviscerated Fish because of Possible Health Risk
Contact: Consumers 1-626-968-8188 (Wednesday to Friday, 1pm to 5pm PST)
Seaquest Seafood Corp. of Industry, California, is recalling its Dehydrated & Marinated Uneviscerated Fish as list below, because they have the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
The recalled items were distributed nationwide in retail stores and through restaurant distributors.
The products come in the corresponding weight listed below in clear plastic package inside a master paper carton with Sunrise Brand on the sides of carton.
No illnesses have been reported to date in connection with this recall.
The potential for contamination was noted after FDA inspection found that the product had not been eviscerated or was under-eviscerated.
- Sunrise Brand Marinated Silver/White Croaker- 30 x 14oz- Barcode 5 08 54336-50081 0
- Sunrise Brand Marinated Climbing Perch- 30 x 16 oz- Barcode 2 08 54336-20130 4
- Sunrise Brand Marinated River Barb- 60 x 10 oz- Barcode 2 08 54336-20140 2
- Sunrise Brand Dehydrated Anchovy size 2/3cm- 1 x 22 lb- Barcode 5 08 54336-50161 9
- Sunrise Brand Dehydrated Anchovy size 3/5cm- 100 x 3.5oz- Barcode 2 08 54336-20161 9
- Sunrise Brand Dehydrated Anchovy size 1/2cm- 1 x 22 lb- Barcode 5 08 54336-50166 4
- Sunrise Brand Dehydrated Big-Eye Herrings- 1 x 3.3 lb- Barcode 5 08 54336-50201 2
Consumers who have purchased the above items are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-626-968-8188 (Wednesday to Friday, 1pm to 5pm PST).
Contact: Consumers 1-626-968-8188 (Wednesday to Friday, 1pm to 5pm PST)
Seaquest Seafood Corp. of Industry, California, is recalling its Dehydrated & Marinated Uneviscerated Fish as list below, because they have the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
The recalled items were distributed nationwide in retail stores and through restaurant distributors.
The products come in the corresponding weight listed below in clear plastic package inside a master paper carton with Sunrise Brand on the sides of carton.
No illnesses have been reported to date in connection with this recall.
The potential for contamination was noted after FDA inspection found that the product had not been eviscerated or was under-eviscerated.
- Sunrise Brand Marinated Silver/White Croaker- 30 x 14oz- Barcode 5 08 54336-50081 0
- Sunrise Brand Marinated Climbing Perch- 30 x 16 oz- Barcode 2 08 54336-20130 4
- Sunrise Brand Marinated River Barb- 60 x 10 oz- Barcode 2 08 54336-20140 2
- Sunrise Brand Dehydrated Anchovy size 2/3cm- 1 x 22 lb- Barcode 5 08 54336-50161 9
- Sunrise Brand Dehydrated Anchovy size 3/5cm- 100 x 3.5oz- Barcode 2 08 54336-20161 9
- Sunrise Brand Dehydrated Anchovy size 1/2cm- 1 x 22 lb- Barcode 5 08 54336-50166 4
- Sunrise Brand Dehydrated Big-Eye Herrings- 1 x 3.3 lb- Barcode 5 08 54336-50201 2
Consumers who have purchased the above items are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-626-968-8188 (Wednesday to Friday, 1pm to 5pm PST).
Thursday, October 22, 2015
New #foodsafety #recall of Rustico Foods Packaged Soup Products that were produced without inspection.
Rustico Foods Recalls Packaged Soup Products Produced Without Benefit of Inspection
Class I Recall130-2015
Health Risk: HighOct 22, 2015
Congressional and Public Affairs
Julie Schwartz
(202) 720-0286
WASHINGTON, Oct. 22, 2015 – Rustico Foods, a Los Angeles, Calif. establishment, is recalling approximately 2,659 pounds of packaged soup products that were produced without the benefit of federal inspection and outside inspection hours, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The ready to eat soups were produced from Sept. 24, 2015, through Oct. 21, 2015. The following products are subject to recall: [View Labels (PDF Only)]
2-lb. individual plastic container of soup labeled “CHICKEN MATZO BALL.”1.6-lb. individual plastic container of soup labeled “CHICKEN MATZO BALL.”1.6-lb. individual plastic container of soup labeled “TURKEY CHILI WITH BEANS.”1.6-lb. individual plastic container of soup labeled “CHICKEN VEGETABLE.”
The products subject to recall bear establishment number “P-45180” inside the USDA mark of inspection. They also bear lot codes “Lot #2662015” through “Lot #2942015” on the bottom of the container and “Best By 10/21/15” through “Best By 11/18/15” stickers on the sides of the container. These items were shipped to retail establishments in southern California.
The problem was discovered when an FSIS Consumer Safety Inspector identified return products that he did not have knowledge of being produced. An FSIS Enforcement Investigations and Analysis Officer then visited the establishment and determined that the establishment also produced some products outside of their approved hours of inspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and media with questions about the recall can contact Jorge Castaneda, Plant Coordinator, at (213) 749-9670.
Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at:http://www.fsis.usda.gov/reportproblem.
USDA Recall ClassificationsClass IThis is a health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.Class IIThis is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.Class IIIThis is a situation where the use of the product will not cause adverse health consequences.
Class I Recall130-2015
Health Risk: HighOct 22, 2015
Congressional and Public Affairs
Julie Schwartz
(202) 720-0286
WASHINGTON, Oct. 22, 2015 – Rustico Foods, a Los Angeles, Calif. establishment, is recalling approximately 2,659 pounds of packaged soup products that were produced without the benefit of federal inspection and outside inspection hours, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The ready to eat soups were produced from Sept. 24, 2015, through Oct. 21, 2015. The following products are subject to recall: [View Labels (PDF Only)]
2-lb. individual plastic container of soup labeled “CHICKEN MATZO BALL.”1.6-lb. individual plastic container of soup labeled “CHICKEN MATZO BALL.”1.6-lb. individual plastic container of soup labeled “TURKEY CHILI WITH BEANS.”1.6-lb. individual plastic container of soup labeled “CHICKEN VEGETABLE.”
The products subject to recall bear establishment number “P-45180” inside the USDA mark of inspection. They also bear lot codes “Lot #2662015” through “Lot #2942015” on the bottom of the container and “Best By 10/21/15” through “Best By 11/18/15” stickers on the sides of the container. These items were shipped to retail establishments in southern California.
The problem was discovered when an FSIS Consumer Safety Inspector identified return products that he did not have knowledge of being produced. An FSIS Enforcement Investigations and Analysis Officer then visited the establishment and determined that the establishment also produced some products outside of their approved hours of inspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and media with questions about the recall can contact Jorge Castaneda, Plant Coordinator, at (213) 749-9670.
Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at:http://www.fsis.usda.gov/reportproblem.
USDA Recall ClassificationsClass IThis is a health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.Class IIThis is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.Class IIIThis is a situation where the use of the product will not cause adverse health consequences.
New #foodsafety #recall of Shuler Meats Turkey Products Packaged due to lack of Inspection
Shuler Meats Recalls Turkey Products Packaged Without the Benefit of Inspection
Class I Recall129-2015
Health Risk: HighOct 22, 2015
WASHINGTON, Oct. 22, 2015 – Shuler Meats, a Thomasville, N.C. establishment, is recalling approximately 25,920 pounds of turkey products that were reconditioned without the benefit of FSIS inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The fully cooked smoked turkey legs were produced from Nov. 24, 2014, through May 4, 2015. The following products are subject to recall: [View Labels (PDF Only)]
648 – 40 lb. (approximate weight) plastic-lined cardboard boxes containing frozen turkey legs with the labels: “Shuler Meats, Co.” and “Belmont Meats, Co.”
The products subject to recall bear establishment number “P-21309” on the Belmont Meats, Co. boxes, and “M-40367” on the Shuler Meats, Co. label. These items were distributed to fairs and retailers in North Carolina and South Carolina.
The problem was discovered when staff from the North Carolina Department of Agriculture notified FSIS personnel of the issue.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and media with questions about the recall can contact Wayne Shuler, owner of Shuler Meats, at (336) 476-6477.
Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at:http://www.fsis.usda.gov/reportproblem.
USDA Recall ClassificationsClass IThis is a health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.Class IIThis is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.Class IIIThis is a situation where the use of the product will not cause adverse health consequences.
Class I Recall129-2015
Health Risk: HighOct 22, 2015
WASHINGTON, Oct. 22, 2015 – Shuler Meats, a Thomasville, N.C. establishment, is recalling approximately 25,920 pounds of turkey products that were reconditioned without the benefit of FSIS inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The fully cooked smoked turkey legs were produced from Nov. 24, 2014, through May 4, 2015. The following products are subject to recall: [View Labels (PDF Only)]
648 – 40 lb. (approximate weight) plastic-lined cardboard boxes containing frozen turkey legs with the labels: “Shuler Meats, Co.” and “Belmont Meats, Co.”
The products subject to recall bear establishment number “P-21309” on the Belmont Meats, Co. boxes, and “M-40367” on the Shuler Meats, Co. label. These items were distributed to fairs and retailers in North Carolina and South Carolina.
The problem was discovered when staff from the North Carolina Department of Agriculture notified FSIS personnel of the issue.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and media with questions about the recall can contact Wayne Shuler, owner of Shuler Meats, at (336) 476-6477.
Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at:http://www.fsis.usda.gov/reportproblem.
USDA Recall ClassificationsClass IThis is a health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.Class IIThis is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.Class IIIThis is a situation where the use of the product will not cause adverse health consequences.
Wednesday, October 21, 2015
Additional #foodsafety #recall possible #botulism contamination of All Canned Salmon Products from VIS Seafoods
VIS Seafoods is Issuing a Voluntary Recall on All Canned Salmon Products Because of a Possible Health Risk
Consumers: 1-360-647-0207
Vis Seafoods of Bellingham, WA is voluntarily recalling ALL canned salmon and smoked salmon with any codes starting with “OC” because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
There have been no reported cases of illness to date.
All products were sold to consumers from our retail store in Bellingham, Washington and sold to internet consumers from the website visseafoods.com. The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with “OC”. The code can be found on either at the bottom or on top of the can. Recalled products are packaged in metal cans with net weight 5.5 oz and 6.0 oz.
Product Name Net Weight UPC
Wild Coho Salmon 6.0 oz. 6 10041 40004 4
Wild Smoked Coho Salmon 6.0 oz. 6 10041 40001 3
Wild King Salmon 6.0 oz. 6 10041 21001 8
Wild Smoked King Salmon 5.5 oz. 6 10041 20001 9
Wild Sockeye Salmon 6.0 oz. 6 10041 10002 9
Wild Smoked Sockeye Salmon 5.5 oz. 6 10041 10001 2
This voluntary recall was initiated after we were notified that our products were possibly under-processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers are advised to destroy or return recalled product to Vis Seafoods for a refund.
If you have any questions, please contact Vis Seafoods at 360-647-0207 between 10am and 6pm PST, Monday –Friday or by email to visseafoods@gmail.com.
Consumers: 1-360-647-0207
Vis Seafoods of Bellingham, WA is voluntarily recalling ALL canned salmon and smoked salmon with any codes starting with “OC” because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
There have been no reported cases of illness to date.
All products were sold to consumers from our retail store in Bellingham, Washington and sold to internet consumers from the website visseafoods.com. The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with “OC”. The code can be found on either at the bottom or on top of the can. Recalled products are packaged in metal cans with net weight 5.5 oz and 6.0 oz.
Product Name Net Weight UPC
Wild Coho Salmon 6.0 oz. 6 10041 40004 4
Wild Smoked Coho Salmon 6.0 oz. 6 10041 40001 3
Wild King Salmon 6.0 oz. 6 10041 21001 8
Wild Smoked King Salmon 5.5 oz. 6 10041 20001 9
Wild Sockeye Salmon 6.0 oz. 6 10041 10002 9
Wild Smoked Sockeye Salmon 5.5 oz. 6 10041 10001 2
This voluntary recall was initiated after we were notified that our products were possibly under-processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers are advised to destroy or return recalled product to Vis Seafoods for a refund.
If you have any questions, please contact Vis Seafoods at 360-647-0207 between 10am and 6pm PST, Monday –Friday or by email to visseafoods@gmail.com.
Additional #foodsafety #recall possible #botulism contamination of All Canned Seafood Products from The Spot of Garibaldi, Oregon
The Spot is Issuing a Voluntary Recall on All Canned Seafood Products Because of a Possible Health Risk
Consumers: 503-322-0080
The Spot of Garibaldi, Oregon is voluntarily recalling ALL canned salmon and tuna with any codes starting with “OC” because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
All products were sold to consumers from our retail store in Oregon. The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with “OC”. The code can be found on either at the bottom or on top of the can. Recalled products are packaged in metal cans with net weight 6 oz. for salmon or 8 oz. for tuna.
Product Name Net Weight Best By Date Range
Spot-On Chinook Salmon 6 oz. No
Spot-On Tuna 8 oz. No
Spot-On Tuna No Salt 8 oz. No
Spot-On Garlic Tuna 8 oz. No
Spot-On Jalapeno Tuna 8 oz. No
Spot-On Smoked Tuna 8 oz. No
There have been no reported cases of illnesses associated with our products to date.
The Spot canned seafood products were made by Skipanon Brand Seafoods LLC and this voluntary recall was initiated after we were notified that that our products were possibly under- processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers who have purchased recalled canned seafood products are urged to destroy or return it to the firm for a full refund.
If you have any questions, please call The Spot at 503-322-0080 between the hours of 10 am and 5 pm PST, Monday-Friday (closed Tuesday).
Consumers: 503-322-0080
The Spot of Garibaldi, Oregon is voluntarily recalling ALL canned salmon and tuna with any codes starting with “OC” because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
All products were sold to consumers from our retail store in Oregon. The last date of distribution of recalled products was September 2015. Affected production codes include any codes starting with “OC”. The code can be found on either at the bottom or on top of the can. Recalled products are packaged in metal cans with net weight 6 oz. for salmon or 8 oz. for tuna.
Product Name Net Weight Best By Date Range
Spot-On Chinook Salmon 6 oz. No
Spot-On Tuna 8 oz. No
Spot-On Tuna No Salt 8 oz. No
Spot-On Garlic Tuna 8 oz. No
Spot-On Jalapeno Tuna 8 oz. No
Spot-On Smoked Tuna 8 oz. No
There have been no reported cases of illnesses associated with our products to date.
The Spot canned seafood products were made by Skipanon Brand Seafoods LLC and this voluntary recall was initiated after we were notified that that our products were possibly under- processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers who have purchased recalled canned seafood products are urged to destroy or return it to the firm for a full refund.
If you have any questions, please call The Spot at 503-322-0080 between the hours of 10 am and 5 pm PST, Monday-Friday (closed Tuesday).
Additional #foodsafety #recall possible #botulism contamination of Brigham Fish Market Canned Seafood Products
Brigham Fish Market is Voluntarily Recalling Canned Seafood Products Because of Possible Health Risk
Consumers: Brigham Fish Market 541-374-9340
This is to inform you that Skipanon Brand Seafoods has initiated a voluntary recall of all its CANNED seafood products. This includes Brigham Fish Market's 6 oz CANNED SMOKED CHINOOK SALMON AND 6 oz CANNED CHINOOK SALMON.
This is due to possible under-processed products. Under-processed products could lead to potentially serious health-risks, and possible contamination with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
There have been no reported cases of illness associated with Skipanon products to date. Notification: Brigham Fish Market canned fish was processed in the same manner.
Consumers who have purchased the 6 oz cans of Brigham Fish Market products are urged to return them to the place of purchase for a full refund.
Consumers with questions can contact Brigham Fish Market; 541-374-9340
Consumers: Brigham Fish Market 541-374-9340
This is to inform you that Skipanon Brand Seafoods has initiated a voluntary recall of all its CANNED seafood products. This includes Brigham Fish Market's 6 oz CANNED SMOKED CHINOOK SALMON AND 6 oz CANNED CHINOOK SALMON.
This is due to possible under-processed products. Under-processed products could lead to potentially serious health-risks, and possible contamination with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
There have been no reported cases of illness associated with Skipanon products to date. Notification: Brigham Fish Market canned fish was processed in the same manner.
Consumers who have purchased the 6 oz cans of Brigham Fish Market products are urged to return them to the place of purchase for a full refund.
Consumers with questions can contact Brigham Fish Market; 541-374-9340
Tuesday, October 20, 2015
Another expanded #foodsafety #recall possible #botulism contamination of Dungeness Seaworks Canned Seafood Products
Dungeness Seaworks is Voluntarily Recalling all Canned Seafood Products Because of Possible Health Risk
Consumers
DUNGENESS SEAWORKS
stjude4@olypen.com
360-683-2898
360-460-7048
Dungeness Seaworks of Sequim, Washington is voluntarily recalling ONLY canned albacore tuna with any code starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
There have been no reported cases of illness to date.
Products were distributed to Nash's Farm Store, Sunny Farms, and Nourish Sequim in Sequim,
WA; Agnew Grocery and Feed in Agnew, WA; Abundantly Green in Poulsbo, WA; and sold at Farmer’s Markets in Poulsbo, WA and in Port Angeles, WA. The last date of distribution of recalled products is September 2015.
Affected production codes include any codes starting with “OC”. The code can be found on either the bottom or on top of the can. Products are packaged in metal cans with 6 ounce net weight cans.
Product Name UPC Brand
Albacore Tuna No UPC Dungeness Seaworks
Albacore Tuna Garlic No UPC Dungeness Seaworks
Albacore Tuna Jalepeno No UPC Dungeness Seaworks
Albacore Tuna Olive Oil No UPC Dungeness Seaworks
Albacore Tuna Hickory Smoke No UPC Dungeness Seaworks
The Dungeness Seaworks products were made by Skipanon Brand Seafoods LLC and this voluntary recall was initiated after we were notified that that our products were possibly under- processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers who have purchased cans of tuna are urged to return it to the place of purchase for a
full refund.
If you have any questions, call DUNGENESS SEAWORKS at 360-683-2898 or 360-460-7048 between the hours of 8:00am PST and 5:00pm PST, Monday- Friday or send e-mail to stjude4@olypen.com
Consumers
DUNGENESS SEAWORKS
stjude4@olypen.com
360-683-2898
360-460-7048
Dungeness Seaworks of Sequim, Washington is voluntarily recalling ONLY canned albacore tuna with any code starting with "OC" because it has the potential to be contaminated with Clostridium botulinum, a bacterium that can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
There have been no reported cases of illness to date.
Products were distributed to Nash's Farm Store, Sunny Farms, and Nourish Sequim in Sequim,
WA; Agnew Grocery and Feed in Agnew, WA; Abundantly Green in Poulsbo, WA; and sold at Farmer’s Markets in Poulsbo, WA and in Port Angeles, WA. The last date of distribution of recalled products is September 2015.
Affected production codes include any codes starting with “OC”. The code can be found on either the bottom or on top of the can. Products are packaged in metal cans with 6 ounce net weight cans.
Product Name UPC Brand
Albacore Tuna No UPC Dungeness Seaworks
Albacore Tuna Garlic No UPC Dungeness Seaworks
Albacore Tuna Jalepeno No UPC Dungeness Seaworks
Albacore Tuna Olive Oil No UPC Dungeness Seaworks
Albacore Tuna Hickory Smoke No UPC Dungeness Seaworks
The Dungeness Seaworks products were made by Skipanon Brand Seafoods LLC and this voluntary recall was initiated after we were notified that that our products were possibly under- processed. The problem was discovered during an inspection at Skipanon Brand Seafoods LLC by the US Food and Drug Administration (FDA).
Consumers who have purchased cans of tuna are urged to return it to the place of purchase for a
full refund.
If you have any questions, call DUNGENESS SEAWORKS at 360-683-2898 or 360-460-7048 between the hours of 8:00am PST and 5:00pm PST, Monday- Friday or send e-mail to stjude4@olypen.com
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