Old Oregon Smokehouse is Issuing a Voluntary Recall Canned Albacore Tuna Because of a Possible Health Risk
Consumers: Old Oregon Smokehouse, 503-355-2817
Old Oregon Smokehouse of Rockaway, Oregon is voluntarily recalling ALL canned Albacore 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.
The recalled product was sold to consumers from our retail stores in Tillamook, Oregon or Rockaway, Oregon. The last date of distribution of recalled product 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 6 oz.
Product Name Net Weight UPC
Albacore Tuna 6 oz. none
There have been no reported cases of illnesses associated with our product to date.
This voluntary recall was initiated after we were notified that our product was 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 who have purchased recalled canned Albacore tuna are urged to destroy or return it to the firm for a full refund.
If you have any questions, please call Old Oregon Smokehouse at 503-355-2817 between the hours of 9 am and 3 pm PST, Monday-Friday.
Tuesday, November 10, 2015
Monday, November 9, 2015
New #foodsafety #recall undeclared #allergen of #chestnuts in Whole Foods Brand Wild Mushroom Soup
Brett Anthony Foods Issues Allergy Alert on Undeclared Chestnuts in Whole Foods Brand Wild Mushroom Soup Sold in Illinois, Indiana, Michigan, Missouri, Minnesota and Nebraska Stores
Consumers: Brett Anthony Foods, 847-272-4309
Brett Anthony Foods of Elk Grove Village Illinois is recalling 109, 24oz cups of Wild Mushroom Soup because it may contain undeclared chestnuts. People who have an allergy or severe sensitivity to chestnuts run the risk of serious or life-threatening allergic reaction if they consume these products.
The Wild Mushroom Soup was sold by Whole Foods Markets in Illinois, Indiana, Michigan, Missouri, Minnesota and Nebraska.
The Wild Mushroom Soup is packaged in a plastic 24oz cup labeled Whole Foods Market, Wild Mushroom Soup. Its expiration date is 112115 located on the bottom of the cups.
NO ILLNESSES HAVE BEEN REPORTED TO DATE
The problem was discovered by a Whole Foods team member upon receipt. The product was discovered to be labeled incorrectly without declaring the allergen.
Consumers who have purchased the Wild Mushroom Soup are urged to return to the place of purchase for a full refund. Consumers with questions may contact the company at 847-272-4309, Monday through Friday, 9:00 to 3:00 CST.
Consumers: Brett Anthony Foods, 847-272-4309
Brett Anthony Foods of Elk Grove Village Illinois is recalling 109, 24oz cups of Wild Mushroom Soup because it may contain undeclared chestnuts. People who have an allergy or severe sensitivity to chestnuts run the risk of serious or life-threatening allergic reaction if they consume these products.
The Wild Mushroom Soup was sold by Whole Foods Markets in Illinois, Indiana, Michigan, Missouri, Minnesota and Nebraska.
The Wild Mushroom Soup is packaged in a plastic 24oz cup labeled Whole Foods Market, Wild Mushroom Soup. Its expiration date is 112115 located on the bottom of the cups.
NO ILLNESSES HAVE BEEN REPORTED TO DATE
The problem was discovered by a Whole Foods team member upon receipt. The product was discovered to be labeled incorrectly without declaring the allergen.
Consumers who have purchased the Wild Mushroom Soup are urged to return to the place of purchase for a full refund. Consumers with questions may contact the company at 847-272-4309, Monday through Friday, 9:00 to 3:00 CST.
New #drug #supplement #recall of Natureal Light green and dark green capsules due to #undeclared #sibutramine
Inaffit, LLC Issues Voluntary Nationwide Recall of Natureal Due to Undeclared Sibutramine
Consumers: Inaffit, LLC, returns@naturealfls.com
Bethesda, MD - Inaffit, LLC is voluntarily recalling all lots of Natureal light green and dark green capsules to the consumer level after FDA laboratory testing found Natureal to contain sibutramine.
Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010. Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. This undeclared ingredient makes this product an unapproved new drug for which safety and efficacy have not been established. This product may also interact in life-threatening ways with other medications a consumer may be taking.
The product is used as a weight loss dietary supplement and is packaged in clear bottle with light green and dark green capsules. The affected Natureal product includes lots Manufactured 3/12/2015 Expiration Date 3/11/2017 which have been distributed from the Natureal office, 14707 South Dixie Highway, Suite 213, Palmetto Bay, FL 33176 and nationwide to consumers via internet www.naturealfls.com.
Inaffit, LLC is notifying its customers by Email and is arranging for return. Consumers who are currently in possession of recalled Natureal light green and dark green capsules should stop using the product and discard. Inaffit, LLC switched to a U.S. Food and Drug Administration Registered Facility to manufacture their dietary supplements and changed the Natureal packaging to a clear bottle with clear capsules.
Consumers with questions regarding this recall can contact Inaffit, LLC by email at returns@naturealfls.com. Consumers should contact their physician or healthcare provider 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: www.fda.gov/medwatch/report.htmdisclaimer icon
Regular Mail or Fax: Download form 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 voluntary recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Consumers: Inaffit, LLC, returns@naturealfls.com
Bethesda, MD - Inaffit, LLC is voluntarily recalling all lots of Natureal light green and dark green capsules to the consumer level after FDA laboratory testing found Natureal to contain sibutramine.
Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010. Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. This undeclared ingredient makes this product an unapproved new drug for which safety and efficacy have not been established. This product may also interact in life-threatening ways with other medications a consumer may be taking.
The product is used as a weight loss dietary supplement and is packaged in clear bottle with light green and dark green capsules. The affected Natureal product includes lots Manufactured 3/12/2015 Expiration Date 3/11/2017 which have been distributed from the Natureal office, 14707 South Dixie Highway, Suite 213, Palmetto Bay, FL 33176 and nationwide to consumers via internet www.naturealfls.com.
Inaffit, LLC is notifying its customers by Email and is arranging for return. Consumers who are currently in possession of recalled Natureal light green and dark green capsules should stop using the product and discard. Inaffit, LLC switched to a U.S. Food and Drug Administration Registered Facility to manufacture their dietary supplements and changed the Natureal packaging to a clear bottle with clear capsules.
Consumers with questions regarding this recall can contact Inaffit, LLC by email at returns@naturealfls.com. Consumers should contact their physician or healthcare provider 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: www.fda.gov/medwatch/report.htmdisclaimer icon
Regular Mail or Fax: Download form 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 voluntary recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
New #foodsafety #recall possible #salmonella contamination of Ground Flax Seed Meal
Zenobia Company LLC. Recalls Ground Flax Seed Meal Because of Possible Health Risk
Consumers: Zenobia Company LLC., 1-877-890-5244
Zenobia Company LLC. of Yonkers, NY is recalling Ground Flax Seed Meal, because they have the potential to be contaminated with Salmonella, 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.
Product was distributed nationwide through online mail order between dates of 6/15/15 - 11/4/15.
This product is labeled Ground Flax Seed Meal packaged in resealable plastic bags of the following sizes: 4 oz. and 16 oz. or 50 pounds bulk. UPC #'s 00575004, 00575016, 00575111
No illnesses have been reported to date.
The recall was initiated after our supplier notified us that the Ground Flax Seed Meal potentially containing Salmonella was shipped to us by them unknowingly.
Consumers with questions may contact the company at 1-877-890-5244, Monday - Friday, 9am - 5pm, EST. Consumers who have purchased Ground Flax Seed Meal are urged to discard product and contact company for a full refund.
Consumers: Zenobia Company LLC., 1-877-890-5244
Zenobia Company LLC. of Yonkers, NY is recalling Ground Flax Seed Meal, because they have the potential to be contaminated with Salmonella, 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.
Product was distributed nationwide through online mail order between dates of 6/15/15 - 11/4/15.
This product is labeled Ground Flax Seed Meal packaged in resealable plastic bags of the following sizes: 4 oz. and 16 oz. or 50 pounds bulk. UPC #'s 00575004, 00575016, 00575111
No illnesses have been reported to date.
The recall was initiated after our supplier notified us that the Ground Flax Seed Meal potentially containing Salmonella was shipped to us by them unknowingly.
Consumers with questions may contact the company at 1-877-890-5244, Monday - Friday, 9am - 5pm, EST. Consumers who have purchased Ground Flax Seed Meal are urged to discard product and contact company for a full refund.
Saturday, November 7, 2015
New #foodsafety #recall undeclared #allergen & #misbranding of Boulder Natural Meats (Beef, Pork, and Poultry Products)
Boulder Natural Meats Recalls Beef, Pork, and Poultry Products Due to Misbranding and Undeclared Allergen
Class I Recall 140-2015
Health Risk: High Nov 7, 2015
Congressional and Public Affairs
Alexandra Tarrant
(202) 720-9113
WASHINGTON, Nov. 7, 2015 – Boulder Natural Meats, a Denver, Colo., establishment, is recalling approximately 3,607 pounds of beef, pork, and poultry products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products were missing the ingredients statement and some contain milk, a known allergen which is not declared on the product label.
The beef, pork, and poultry products were produced on various dates. The following products are subject to recall: [View Labels (PDF only)]
10 lb. vacuum sealed packages of “BN CHICKEN MILD ITALIAN SAUSAGE”
10 lb. vacuum sealed packages of “BN CHICKEN HOT ITALIAN SAUSAGE”
10 lb. vacuum sealed packages of “BN CHICKEN BREAKFAST SAUSAGE”
10 lb. vacuum sealed packages of “FRESH CHICKEN CHORIZO SAUSAGE”
8 lb. vacuum sealed packages of “COWBOY BURGERS ASPEN NATURAL MEATS”
16 oz. plastic frozen tubs of “CHICKEN LIVERS”
8 lb. vacuum sealed packages of “BACON & CHEDDAR CHEESE SEASONED BEEF BURGERS ASPEN NATURAL MEATS”
8 lb. vacuum sealed packages of “SMOKED SALT & BALINESE PEPPER SEASONED BURGERS ASPEN NATURAL MEATS”
10 lb. vacuum sealed packages of “BN PORK HOT ITALIAN SAUSAGE”
10 lb. vacuum sealed packages of “BN PORK MILD ITALIAN SAUSAGE
10 lb. vacuum sealed packages of “BN PORK SAGE BREAKFAST SAUSAGE”
10 lb. vacuum sealed packages of “BN PORK CHORIZO SAUSAGE”
The products subject to recall bear establishment number “EST. 18852” and “P-18852” inside the USDA marks of inspection. These items were shipped to one distributor and retail stores in Kansas, Missouri, and Oklahoma.
The problem was discovered by an FSIS investigator who observed misbranded meat products at a retail store.
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 Boulder Natural Meats at (570) 600-2996.
Class I Recall 140-2015
Health Risk: High Nov 7, 2015
Congressional and Public Affairs
Alexandra Tarrant
(202) 720-9113
WASHINGTON, Nov. 7, 2015 – Boulder Natural Meats, a Denver, Colo., establishment, is recalling approximately 3,607 pounds of beef, pork, and poultry products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products were missing the ingredients statement and some contain milk, a known allergen which is not declared on the product label.
The beef, pork, and poultry products were produced on various dates. The following products are subject to recall: [View Labels (PDF only)]
10 lb. vacuum sealed packages of “BN CHICKEN MILD ITALIAN SAUSAGE”
10 lb. vacuum sealed packages of “BN CHICKEN HOT ITALIAN SAUSAGE”
10 lb. vacuum sealed packages of “BN CHICKEN BREAKFAST SAUSAGE”
10 lb. vacuum sealed packages of “FRESH CHICKEN CHORIZO SAUSAGE”
8 lb. vacuum sealed packages of “COWBOY BURGERS ASPEN NATURAL MEATS”
16 oz. plastic frozen tubs of “CHICKEN LIVERS”
8 lb. vacuum sealed packages of “BACON & CHEDDAR CHEESE SEASONED BEEF BURGERS ASPEN NATURAL MEATS”
8 lb. vacuum sealed packages of “SMOKED SALT & BALINESE PEPPER SEASONED BURGERS ASPEN NATURAL MEATS”
10 lb. vacuum sealed packages of “BN PORK HOT ITALIAN SAUSAGE”
10 lb. vacuum sealed packages of “BN PORK MILD ITALIAN SAUSAGE
10 lb. vacuum sealed packages of “BN PORK SAGE BREAKFAST SAUSAGE”
10 lb. vacuum sealed packages of “BN PORK CHORIZO SAUSAGE”
The products subject to recall bear establishment number “EST. 18852” and “P-18852” inside the USDA marks of inspection. These items were shipped to one distributor and retail stores in Kansas, Missouri, and Oklahoma.
The problem was discovered by an FSIS investigator who observed misbranded meat products at a retail store.
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 Boulder Natural Meats at (570) 600-2996.
New #foodsafety #recall undeclared #allergen & #misbranding of Cloverdale Foods beef and pork jalapeño cheddar bratwurst product
Cloverdale Foods Company Recalls Beef and Pork Product Due to Misbranding and Undeclared Allergen
Class I Recall 139-2015
Health Risk: High Nov 7, 2015
Congressional and Public Affairs
Alexandra Tarrant
(202) 720-9113
WASHINGTON, Nov. 7, 2015 – Cloverdale Foods Company, a Mandan, ND, establishment, is recalling approximately 5,208 pounds of beef and pork jalapeño cheddar bratwurst product due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product was incorrectly labeled as beef frankfurters and contains milk, a known allergen which is not declared on the product label.
The beef and pork bratwurst product was produced on Sept. 21, 2015, and Oct. 2, 2015. The following product is subject to recall: [View Label (PDF only)]
10 oz. packages labeled as “TETON WATERS RANCH UNCURED BEEF FRANKFURTERS” with the use by dates of “12/5/15” and “12/16/15”
The product subject to recall bears establishment number “EST. 7603” inside the USDA mark of inspection. These items were shipped to three distributors and then distributed nationwide.
The problem was discovered by a consignee of Cloverdale Foods Company during a store audit. The company then notified FSIS.
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 Scott Russell, Executive Vice President, at (701) 663-9511 ext. 224.
Class I Recall 139-2015
Health Risk: High Nov 7, 2015
Congressional and Public Affairs
Alexandra Tarrant
(202) 720-9113
WASHINGTON, Nov. 7, 2015 – Cloverdale Foods Company, a Mandan, ND, establishment, is recalling approximately 5,208 pounds of beef and pork jalapeño cheddar bratwurst product due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product was incorrectly labeled as beef frankfurters and contains milk, a known allergen which is not declared on the product label.
The beef and pork bratwurst product was produced on Sept. 21, 2015, and Oct. 2, 2015. The following product is subject to recall: [View Label (PDF only)]
10 oz. packages labeled as “TETON WATERS RANCH UNCURED BEEF FRANKFURTERS” with the use by dates of “12/5/15” and “12/16/15”
The product subject to recall bears establishment number “EST. 7603” inside the USDA mark of inspection. These items were shipped to three distributors and then distributed nationwide.
The problem was discovered by a consignee of Cloverdale Foods Company during a store audit. The company then notified FSIS.
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 Scott Russell, Executive Vice President, at (701) 663-9511 ext. 224.
Friday, November 6, 2015
New #petfood #recall of Blue Buffalo Kitty Yums Chicken Recipe Cat Treats Due to the Presence of Propylene Glycol
Blue Buffalo Company, Ltd. Voluntarily Recalls Limited Production of Kitty Yums Chicken Recipe Cat Treats Due to the Presence of Propylene Glycol
Consumers: Blue Buffalo: BlueBuffalo5883@stericycle.com
888-667-1508
Blue Buffalo Company, Ltd. is voluntarily recalling a limited production of Blue Kitty Yums Chicken Recipe Cat Treats that may contain low levels of propylene glycol, which is not permitted by the FDA for use in cat food.
Cats reacting to high doses of propylene glycol may exhibit signs of depression and may have a loss of coordination, muscle twitching, and excessive urination and thirst. If your cat has consumed the recalled product and has these symptoms, please contact your veterinarian.
The affected product was distributed nationwide in the US and Canada through pet specialty stores and e-commerce.
The product is packaged in a 2 oz., plastic stand up pouch. Only these specific code dates of this product are involved:
Blue Kitty Yums Tasty Chicken Recipe, UPC: 859610007820 - Best If Used By: April 24, 2016.
Blue Kitty Yums Tasty Chicken Recipe, UPC: 859610007820 - Best If Used By: July 24, 2016.
No other BLUE pet foods or treats are involved in this recall.
The FDA tested product in response to a single consumer complaint and found propylene glycol in one bag of our cat treats in the impacted lot. To date we have had no other reports of incidents related to our cat treats. Out of an abundance of caution, we are voluntarily recalling all product manufactured in the same lot as the subject bag.
Consumers who have purchased the product being recalled may return it to the place of purchase for a full refund. Consumers with questions may contact Blue Buffalo at: 888-667-1508 from 8 AM to 5 PM Eastern Time Monday through Friday and the weekend of November 7, 2015 or by email at BlueBuffalo5883@stericycle.com for more information.
About Blue Buffalo
Blue Buffalo, based in Wilton, CT, is a pet products company that makes natural foods and treats for pets.
Consumers: Blue Buffalo: BlueBuffalo5883@stericycle.com
888-667-1508
Blue Buffalo Company, Ltd. is voluntarily recalling a limited production of Blue Kitty Yums Chicken Recipe Cat Treats that may contain low levels of propylene glycol, which is not permitted by the FDA for use in cat food.
Cats reacting to high doses of propylene glycol may exhibit signs of depression and may have a loss of coordination, muscle twitching, and excessive urination and thirst. If your cat has consumed the recalled product and has these symptoms, please contact your veterinarian.
The affected product was distributed nationwide in the US and Canada through pet specialty stores and e-commerce.
The product is packaged in a 2 oz., plastic stand up pouch. Only these specific code dates of this product are involved:
Blue Kitty Yums Tasty Chicken Recipe, UPC: 859610007820 - Best If Used By: April 24, 2016.
Blue Kitty Yums Tasty Chicken Recipe, UPC: 859610007820 - Best If Used By: July 24, 2016.
No other BLUE pet foods or treats are involved in this recall.
The FDA tested product in response to a single consumer complaint and found propylene glycol in one bag of our cat treats in the impacted lot. To date we have had no other reports of incidents related to our cat treats. Out of an abundance of caution, we are voluntarily recalling all product manufactured in the same lot as the subject bag.
Consumers who have purchased the product being recalled may return it to the place of purchase for a full refund. Consumers with questions may contact Blue Buffalo at: 888-667-1508 from 8 AM to 5 PM Eastern Time Monday through Friday and the weekend of November 7, 2015 or by email at BlueBuffalo5883@stericycle.com for more information.
About Blue Buffalo
Blue Buffalo, based in Wilton, CT, is a pet products company that makes natural foods and treats for pets.
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