New #foodsafety #recall possible #Ecoli #contamination of Select Golden Temple®, Swad®, and Maya® Flour Products

Smucker Foods of Canada Corp. Announces a Voluntary Recall on Select Golden Temple®, Swad®, and Maya® Flour Products in the U.S. Due to Possible E. Coli 0121 Contamination

For Immediate Release

May 31, 2017

Contact

Consumers

 1-888-569-6728

 

Announcement

View Product Photos

Markham, ON Canada – In collaboration with the U.S. Food and Drug Administration (FDA), Smucker Foods of Canada Corp. today announced a voluntary recall on specific production codes of Golden Temple®, Swad®, and Maya® flour products in the U.S. due to possible E. coli 0121 contamination.

The impacted product was produced by Ardent Mills located in Saskatoon, SK Canada. Additional flour and flour products have been voluntarily recalled in Canada in cooperation with the Canadian Food Inspection Agency as part of their ongoing E. Coli investigation.

No other Smucker Foods of Canada Corp. products distributed in the U.S. are affected by this recall.

Impacted product is packaged in 20 lb. paper bags and was distributed nationwide to 19 distributors and two small retailers.

Some strains of E. coli create potentially deadly bacterium that can cause bloody diarrhea and dehydration. 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 and those with compromised immune systems. The condition can lead to serious kidney failure and even death. Any consumers concerned about an illness should contact a physician.

There are no reported illnesses to date associated with the U.S. product recall.

If you have any of the products listed below, please dispose of them immediately. Consumers with impacted product are urged to contact the company at 1-888-569-6728 Monday through Friday 8:00 AM – 5:00 PM ET for a product replacement coupon.  
 

Product Description	Size	UPC Code	Lot Codes	Best By Date
Maya® Durum Wheat Atta Flour	20 lbs	0 20843 10001 9	6 286 548  6 287 548	No BIUB on Bag No BIUB on Bag
Swad® Durum Atta Flour Chappati Flour	20 lbs	0 51179 16030 9	6 294 548 6 299 548 6 300 548 6 308 548	No BIUB on Bag No BIUB on Bag No BIUB on Bag No BIUB on Bag
Golden Temple® #1 Fine Durum Atta Flour Blend	20 lbs	0 59000 40540 7	6 286 548 6 299 548	Best if Use By Jan 2018 Best if Use By Jan 2018
Golden Temple® Durum Atta Flour Blend	20 lbs	0 59000 41556 7	6 287 548 6 288 548 6 294 548 6 295 548 6 300 548 6 301 548 6 306 548 6 307 548 6 308 548	Best if Use By Jan 2018 Best if Use By Jan 2018 Best if Use By Jan 2018 Best if Use By Jan 2018 Best if Use By Jan 2018 Best if Use By Jan 2018 Best if Use By Feb 2018 Best if Use By Feb 2018 Best if Use By Feb 2018

The FDA offers these tips for safe flour handling and usage:

• Recalled products should be placed in a sealed plastic bag and discarded.
• Do not eat any raw cookie dough, cake mix, batter, or any other raw dough or batter product.
• Wash hands, work surfaces, and utensils thoroughly after contact with flour and raw dough products.

The recall is being conducted in cooperation with the U.S. Food and Drug Administration.

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New #foodsafety #recall of 45,985 pounds of beef trimming products due to possible adulteration

Readfield Meats, Inc. Recalls Beef Trimming Products Due to Possible Adulteration

Class II Recall057-2017

Health Risk: LowMay 27, 2017

En Español

Congressional and Public Affairs
Mitch Adams
(202) 720-9113
Press@fsis.usda.gov

WASHINGTON, May 27, 2017 – Readfield Meats, Inc., doing business as Ruffino Meats & Food Service, a Bryan, Texas establishment, is recalling approximately 45,985 pounds of beef trimming products due to possible adulteration, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product labels include “For Cooking Only,” indicating that they are intended for further processing to apply a full lethality at a federally inspected establishment. Because the products were distributed to non-federally inspected establishments where it cannot be verified that sufficient further processing occurred to remove foodborne pathogens that could have been present, these products must be removed from commerce.

The frozen raw beef trimmings items were produced from May 26, 2015 through May 26, 2017. The following products are subject to recall: [View Labels (PDF Only)]

• 50-lb. boxes containing “BEEF TRIMMINGS FOR COOKING ONLY.”

The products subject to recall bear establishment number “EST. 13126” inside the USDA mark of inspection. These items were shipped to retail markets, state inspected plants, and individuals located in Texas.

The problem was discovered when an FSIS compliance officer found cases of raw beef trimmings labeled “For Cooking Only” at a retail location.

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.

Consumers and media with questions about the recall can contact Terry Wiese, plant manager, at (979) 776-5685.

New #foodsafety #recall of 5,163 lbs of beef broth products produced without inspection

Cauldron Soups, LLC Recalls Beef Broth Products Produced Without Benefit of Inspection

Class I Recall056-2017

Health Risk: HighMay 26, 2017

En Español

Congressional and Public Affairs
Mitch Adams
(202) 720-9113
Press@fsis.usda.gov

WASHINGTON, May 26, 2017 – Cauldron Soups, LLC, doing business as Cauldron Broths, a Bellingham, Wash. establishment, is recalling approximately 5,163 pounds of beef broth products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The beef bone broth items were produced and packaged between December 21, 2016 and May 22, 2017. The following products are subject to recall: [View Labels (PDF Only)]       

• 24-fl. oz. individual plastic pouches containing “Vital Choice GRASS-FED BEEF BONE BROTH” with best by dates 1/15/2018, 1/18/2018 and 3/28/2018.
• 24-fl. oz. individual plastic pouches containing “CAULDRON BROTHS BEEF BONE BROTH” with best by dates 1/3/18 and 2/15/18.
• 24-fl. oz. individual plastic pouches containing “CAULDRON BROTHS ORGANIC CAULDRON'S CURE” with best by dates 12/21/18.
• 1-gal. individual plastic containers containing “CAULDRON BROTHS GLACE DE VIANDE” with best by date 1/30/18.
• 8-fl. oz. individual plastic containers containing “CAULDRON BROTHS GLACE DE VIANDE” with best by date 3/4/18.

The products subject to recall bear establishment number “EST. 45953” inside the USDA mark of inspection. These items were shipped to retail locations in the state of Washington and to a distributor who conducts internet sales direct to consumers nationwide.

The problem was discovered when FSIS personnel found FSIS product that was produced without FSIS inspection.

There have been no confirmed reports of adverse reactions or illness due to consumption of these products. Anyone concerned about a reaction 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 Gabriel Claycamp, CEO, at (360) 671-1098 or by email at customercare@cauldronbroths.com.

New #foodsafety #recall possible #Listeria #contamination of Simple Truth Dry Roasted Macadamia Nuts

Kroger Recalls Simple Truth Dry Roasted Macadamia Nuts Because of Possible Health Risk

For Immediate Release

May 24, 2017

Contact

Consumers

 1-800-KROGERS

Media

Kristal Howard
 (513) 762-1304

Announcement

View Product Photos

The Kroger Co. (NYSE: KR) today announced the recall of its Simple Truth Dry Roasted Macadamia Nuts due to potential Listeria monocytogenes contamination.  A supplier reported the product may have 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.  No customer illnesses have been reported to date.

The product comes in a 12 ounce, clear plastic package marked with an expiration date of May 02, 2018 stamped on the side.  Kroger has removed the following item from store shelves and initiated its customer recall notification system that alerts customers who may have purchased recalled Class 1 products through register receipt tape messages and phone calls.

Product	UPC	Code	Size
Simple Truth Dry Roasted Macadamia Nuts	11110-02478	Sell By:  May 02 2018	12 oz.

Kroger, Bakers, Gerbes and Dillons stores operating in the following states are included in this recall: Ohio, Southeast Indiana, Northern Kentucky, Kansas, Nebraska and Missouri.

Customers who have purchased any of the products described above should not consume them and should return them to a store for a full refund or replacement.

Customers who have questions may contact Kroger at 1-800-KROGERS, Monday through Friday 8:00 a.m. to 12:00 a.m. ET and Saturday through Sunday 8:00 a.m. to 9:00 p.m. ET.

Every day, the Kroger Family of Companies makes a difference in the lives of eight and a half million customers and 443,000 associates who shop or serve in 2,796 retail food stores under a variety of local banner names in 35 states and the District of Columbia. Kroger and its subsidiaries operate an expanding ClickList offering – a personalized, order online, pick up at the store service – in addition to our 2,255 pharmacies, 784 convenience stores, 319 fine jewelry stores, 220 retail health clinics, 1,445 supermarket fuel centers and 38 food production plants in the United States. Kroger is recognized as one of America’s most generous companies for its support of more than 100 Feeding America food bank partners, breast cancer research and awareness, the military and their families, and more than 145,000 community organizations including schools. A leader in supplier diversity, Kroger is a proud member of the Billion Dollar Roundtable.

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New #foodsafety #recall #undeclared #milk #allergen in Kroger Yellow Sponge Cake Dessert Cups

Kroger Issues Allergy Alert on Undeclared Milk in Kroger Yellow Sponge Cake Dessert Cups

For Immediate Release

May 24, 2017

Contact

Consumers

 1-800-KROGERS

Media

Kristal Howard
 (513) 762-1304

Announcement

View Product Photos

The Kroger Co. has recalled Kroger Dessert Cups –Yellow Sponge Cake (6.5 oz., 6 Pack) sold in its retail stores because it contains undeclared milk.  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.  Although milk is listed in the ingredient statement, milk is not included in the “Contains” statement.

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.  For consumers who are not sensitive to milk, there is no safety issue with the product.  This recall was initiated because Kroger was notified of this issue by a customer who consumed this product. One customer illness has been reported at this time.

All stores operating under names Kroger, Owen’s, Pay Less, Scott’s, Gerbes, Ruler Foods, Dillons, Baker’s, Food4Less and  Jay C, located in Alabama, Arkansas, Georgia, Illinois, Indiana, Kansas, Kentucky, Michigan, Mississippi, Missouri, Nebraska, North Carolina, Ohio, South Carolina, Tennessee, Virginia and West Virginia.

Kroger is recalling the following item:

Product	Consumer UPC	Codes	Size
Kroger Dessert Cups – Yellow Sponge Cake, 6-pack	11110-18550	All Codes	6.5 oz.

Customers who have purchased any of the products described above should not consume them and should return them to a store for a full refund or replacement.

Customers who have questions may contact Kroger at 1-800-KROGERS, Monday through Friday 8:00 a.m. to 12:00 a.m. ET and Saturday through Sunday 8:00 a.m. to 9:00 p.m. ET.

Every day, the Kroger Family of Companies makes a difference in the lives of eight and a half million customers and 443,000 associates who shop or serve in 2,796 retail food stores under a variety of local banner names in 35 states and the District of Columbia. Kroger and its subsidiaries operate an expanding ClickList offering – a personalized, order online, pick up at the store service – in addition to our 2,255 pharmacies, 784 convenience stores, 319 fine jewelry stores, 220 retail health clinics, 1,445 supermarket fuel centers and 38 food production plants in the United States. Kroger is recognized as one of America’s most generous companies for its support of more than 100 Feeding America food bank partners, breast cancer research and awareness, the military and their families, and more than 145,000 community organizations including schools. A leader in supplier diversity, Kroger is a proud member of the Billion Dollar Roundtable.
 

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New #foodsafety #recall possible #Listeria #contamination of Ava's Brand Organic Cashews Roasted & Salted 8 oz. Tubs in NJ, NY, PA and CT

Recall on Fewer Than 225 Ava's Brand Organic Cashews Roasted & Salted 8 oz. Tubs in NJ, NY, PA and CT

For Immediate Release

May 26, 2017

Contact

Consumers

 413-732-4193, press 0

 

Announcement

View Product Photos

Hampton Farms is voluntarily recalling Ava's brand Organic Cashews Roasted & Salted 8 oz. tubs distributed in New Jersey, New York, Pennsylvania and Connecticut. We have been notified by our cashew supplier that the cashews used have the potential to be contaminated with Listeria monocytogenes. No confirmed illnesses have been reported to public health authorities to date. Routine sampling of a different item from another company revealed positive Listeria monocytogenes results, and a subsequent investigation in their manufacturing environment revealed a contaminated piece of equipment that was also used to produce the ingredient we received. Although test results of our cashews were negative for Listeria, we are recalling this item out of an abundance of caution.

All affected distributors and retail stores have been notified and the affected products are being removed from store shelves. Fewer than 225 units of this product were offered for retail sale.

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.

This announcement applies only to the Ava's brand Organic Cashews Roasted & Salted product listed below and does not include any other items or the same item outside of this lot code:

Ava's Brand 8 oz. Organic Roasted Salted Cashews
UPC 8-10111-01035-1
Best By 4/28/18, Lot 11817-L2

No other Ava's branded products or any other products produced by Hampton Farms are included within this recall.

Consumers should not consume these products. Affected product may be returned to the place of purchase for a full refund. Consumers with questions may contact Hampton Farms at 413-732-4193, press 0.

This recall is being undertaken with the knowledge of the Food and Drug Administration. "We deeply regret this situation and have employed our established recall plan to immediately remove the product from distribution. Nothing is more important than providing safe and wholesome, quality products," said Dallas Barnes, President of Hampton Farms.

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New #foodsafety #recall Undeclared #milk & #ED meds in Caverflo Natural Herbal Coffee

Caverflo.com Issues Voluntary Nationwide Recall of Caverflo Natural Herbal Coffee due to the Presence of Undeclared Active Pharmaceutical Ingredients and Undeclared Milk

For Immediate Release

May 25, 2017

Contact

Consumers

Caverflo.com 
  coffeekingb@yahoo.com
 214-803-4652

Media

Brian Richardson
 214 803-4652

Announcement

Caverflo.com is voluntarily recalling all lots of Caverflo Natural Herbal Coffee, 25 grams to the consumer level. FDA laboratory analysis confirmed the presence of Sildenafil and Tadalafil which are the active ingredients in two FDA-approved prescription drugs used for the treatment of erectile dysfunction (ED). Caverflo.com has received a report of an individual death after use of the coffee. Caverflo Natural Herbal Coffee may also contain undeclared milk.

These undeclared ingredients may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. Men with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. People who have an allergy or severe sensitivity to milk run the risk of serious or life threatening allergic reaction if they consume this product.

Caverflo Natural Herbal Coffee is used as a male enhancement and is packaged in 25 gram black foil packs, UPC 9555671709994. Caverflo.com distributed this product from August 2016 through February 2017. Caverflo Natural Herbal Coffee is consumed as an instant coffee. Caverflo Natural Herbal Coffee was distributed nationwide to consumers via internet at Caverflo.com.

Caverflo.com is notifying its customers by email. Consumers that have Caverflo Natural Herbal Coffee which is being recalled should stop using/discard/ and contact their doctor.

Consumers with questions regarding this recall can contact Caverflo.com at 214-803-4652 or coffeekingb@yahoo.com Monday thru Friday 9am to 5pm CST. 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.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

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

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New #foodsafety #recall #undeclared #almond & #milk #allergen in California Sun Dry Sun-Dried Tomato Pesto

California Sun Dry Foods Announces a Voluntary Recall of Mislabeled California Sun Dry Sun-Dried Tomato Pesto Due to Undeclared Almond and Milk Allergen

For Immediate Release

May 25, 2017

Contact

Consumers

California Sun Dry Foods
 1-800-995-7753

Announcement

View Product Photos

California Sun Dry Foods today issued a voluntary recall of California Sun Dry Sun-Dried Tomato Pesto because of a potentially incorrect back label on some jars. This mislabeling incident resulted in undeclared allergens (Almonds and Milk). People who have an allergy or severe sensitivity to tree nuts and milk run the risk of serious or life-threatening allergic reaction if they consume this product.

The front of the jar is correctly labeled California Sun Dry Sun-Dried Tomato Pesto, 8.5 oz. However, the back of some jars may be incorrectly labeled California Sun Dry Sun-Dried Tomato Garlic, UPC# 7-38203-10911-3. One Code Date is affected: PTP0567A USE BY 25FEB2019 printed on the cap.

The recall was immediately initiated after a California Sun Dry Foods employee discovered a mislabeled jar at the store while building a display case.

The product involved was distributed through retail stores nationwide.

No illnesses have been reported to date in association with this product.

Consumers can return the product to their place of purchase for a full refund. Consumers with questions can contact California Sun Dry Foods at 1 (800) 995-7753 8am to 5pm PDT, Monday-Friday.

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New #foodsafety #recall possible #Listeria #contamination of 5,248 lb of frozen Waffle and Turkey Sausage products

Golden Gourmet Recalls Frozen Waffle and Turkey Sausage Products Due to Possible Listeria Contamination

Class I Recall055-2017

Health Risk: HighMay 25, 2017

En Español

Congressional and Public Affairs
Autumn Canaday
(202) 720-9113
Press@fsis.usda.gov

WASHINGTON, May 25, 2017 – Golden Gourmet, an Americus, Ga. establishment, is recalling approximately 5,248 pounds of frozen entree products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The frozen waffles with turkey sausage patty items were produced and packaged on December 21, 2016, December 28, 2016, December 29, 2016 and December 30, 2016. The following products are subject to recall: [View Labels (PDF Only)]   

•  5,248 lbs. of 7.1 oz. trays with clear film in cardboard box packages containing “Waffles, Turkey Sausage Patty with Sliced Apple Seasoned w/Brown Sugar and Cinnamon” on the label, lot codes of  “2016355,” “2016363,” “2016364” and “2016362,” and Use By dates of  06/21/18, 06/28/18, 06/29/18 and 06/30/18.

The products subject to recall bear establishment number “P-51269” inside the USDA mark of inspection. These items were shipped to institutions in Georgia, Iowa, Illinois, Ohio, South Carolina and Tennessee.

The problem was discovered on May 19, 2017 when Golden Gourmet was notified by their supplier that the waffles used in the waffle and turkey sausage products were recalled due to potential Lm contamination.  Golden Gourmet notified FSIS on May 23, 2017. 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.

Media and consumers with questions regarding the recall can contact Sherry Cannon, office manager, at (229) 389-2392.

New #foodsafety #recall possible metal #contamination of 90,978 lbs of ready-to-eat sausage products

Armour Eckrich Meats, LLC Recalls Ready-To-Eat Sausage Products Due to Possible Foreign Matter Contamination

Class II Recall054-2017

Health Risk: LowMay 24, 2017

Congressional and Public Affairs
Autumn Canaday 
(202) 720-9113
Press@fsis.usda.gov

WASHINGTON, May 24, 2017– Armour Eckrich Meats, LLC, a Junction City, Kan. establishment, is recalling approximately 90,978 pounds of ready-to-eat sausage products that may be contaminated with extraneous materials, specifically pieces of metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The food service fully-cooked pork, turkey and beef breakfast sausage items were produced and packaged from April 26 through April 28, 2017. The following products are subject to recall: [View Labels (PDF Only)]

• 8,769 cases of 16.6 oz. vacuumed packages containing “ECKRICH SMOK-Y CHEDDAR BREAKFAST SAUSAGE, NATURALLY HARDWOOD SMOKED” on the label, case code/ UPC number “27815 17984,” and a Use By date of “08/17/17.”

The products subject to recall bear establishment number “EST. 3JC” inside the USDA mark of inspection. These items were shipped to distribution centers in Arkansas, Indiana, Kansas, Louisiana, Oklahoma and Texas.

The problem was discovered on May 15, 2017 when Armour Eckrich Meats, Inc. was notified by another FSIS-regulated establishment that pieces of metal were embedded in a fully cooked sausage product produced by Armour Eckrich Meats, Inc.

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.

Consumers with questions about the recall can call 1 (877) 933-4625. Media with questions about the recall can contact Kassi Belz, vice president of public relations for the Dalton Agency, at (904) 398-5222.