Tag Archives: recalls

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USDA FSIS: Night Hawk Frozen Foods recalls frozen beef patty and gravy products due to misbranding and undeclared allergens

WASHINGTON, 2018-Feb-22 — /EPR Retail News/ — Night Hawk Frozen Foods, Inc., a Buda, Texas establishment, is recalling approximately 167 pounds of frozen beef patty and gravy products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (Feb. 20, 2018). The product contains milk, a known allergen, which is not declared on the product label.

The heat treated, but not fully cooked, frozen beef patty and gravy items were produced on Nov. 8, 2017. The following products are subject to recall:

  • 8.75 oz. board cartons labeled as “NIGHT HAWK BEEF PATTY ‘N GRAVY, CHARBROILED BEEF PATTY and GRAVY, POTATO ROUNDS and SWEET CORN.”

The products subject to recall bear establishment number “EST. 2117” inside the USDA mark of inspection. These items were shipped to retail locations in Louisiana and Texas.

The problem was discovered on Feb. 19, 2018 when FSIS was notified that the firm received two consumer complaints of mislabeled products. The cartons actually contain beef patties, mashed potatoes and cheese.

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 Michelle Anselment, chief operating officer, Night Hawk Frozen Foods, at (512) 295-4166 X 107.

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 10 a.m. to 6 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: https://www.fsis.usda.gov/reportproblem.

USDA Recall Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

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

Source: USDA

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Santa Fe Importers recalls pork salami products that may be contaminated with extraneous materials

WASHINGTON, 2017-Dec-13 — /EPR Retail News/ — Santa Fe Importers, Inc. a Long Beach, Calif. establishment, is recalling approximately 143 pounds of pork salami products that may be contaminated with extraneous materials, specifically metal shavings, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (Dec. 12, 2017).

The pork salami items were produced on Aug. 3, 2017. The following products are subject to recall: 

  • 3.5 to 4.0-lbs. random weight of plastic wrapped packages of “MARISA PREMIUM QUALITY GENOA SALAMI ITALIAN BRAND,” with a packaging date of Sept. 14, 2017 and a lot code of 257-100161 in the upper right hand corner.

The products subject to recall bear establishment number “EST. 4118” inside the USDA mark of inspection. These items were shipped to retail locations in California.

The problem was discovered after the company received a complaint from their retail customer and notified FSIS on Dec. 11, 2017.

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 contact Vincent Passanisi, president, at (562) 437-7775. Media with questions about the recall can contact Jorge Endara, general manager, at (562) 437-7775.

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 10 a.m. to 6 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 Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

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

Source: USDA

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Casa Sanchez Foods recalls “Real Guacamole” that may be contaminated with Listeria monocytogenes

Casa Sanchez Foods recalls “Real Guacamole” that may be contaminated with Listeria monocytogenes

 

Hayward, CA, 2017-Nov-17 — /EPR Retail News/ — Casa Sanchez Foods of Hayward, CA, is recalling its 9-ounce containers of “Real Guacamole” because they 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.

The recalled “Real Guacamole” was distributed to retail stores throughout the California Bay Area and surrounding counties.

This recalled product is packaged in 9-ounce, clear plastic containers that are labeled with the following information:

Front Label – Casa Sanchez Foods, Real Guacamole, UPC # 0 78732 00412 2
Bottom Label – White sticker showing the manufacturing lot code 279 and the product expiration date of 11/10/17.

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

This issue was identified after FDA product sampling identified Listeria monocytogenes in the product.

The current manufacturing process of this product has been suspended while the FDA and the company continue to investigate the source of the issue.

Consumers who have purchased 9-ounce containers of “Real Guacamole” with manufacturing lot code 279 are urged to return them to the place of purchase for a full refund.

Consumers with questions may contact the company at 1-877-227-2726 between the hours of 8:00 am and 5:00 pm PST.

Consumers Contact:

1-877-227-2726

Media Contact:

Robert Sanchez
650-697-7525

Source: FDA

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Sukhi’s Gourmet Indian Foods recalls chicken tikka masala products that may be adulterated with Listeria monocytogenes

WASHINGTON, 2017-Nov-15 — /EPR Retail News/ — Sukhi’s Gourmet Indian Foods, a Hayward, Calif. establishment, is recalling approximately 264 pounds of chicken tikka masala products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (Nov. 14, 2017).

The cooked ready-to-eat (RTE) chicken tikka masala items were produced on Nov. 7, 2017. The following products are subject to recall: 

  • 11-oz. frozen microwaveable sealed containers of “Sukhi’s CHICKEN TIKKA MASALA with NAAN BREAD & BASMATI RICE” with a “USE BY” date of 11/07/2018 and lot number 83790.

The products subject to recall bear establishment number “P-44187” on the side of the individual product cartons. These items were shipped to a distributor in California.

The problem was discovered on Nov. 13, 2017 when the Alameda district office received notification that the firm shipped adulterated product into commerce. Specifically, a sample of the product was collected by FSIS personnel on Nov. 7, 2017 and was confirmed to be positive with Listeria monocytogenes on Nov. 13, 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 with questions regarding the recall can contact Storrie Johnson, Chief Supply Chain Officer, at (510) 316-9409. Consumers with questions regarding the recall can contact Donna Soares, Director of Customer Service, at (510) 336-8372.

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 10 a.m. to 6 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 Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

Contact:
Congressional and Public Affairs
Brett Filloon
(202) 720-9113
Press@fsis.usda.gov

Source: USDA

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Seattle Gourmet Foods recalls Dilettante Chocolates Espresso Blend, Espresso Beans may contain undeclared almonds

Seattle Gourmet Foods recalls Dilettante Chocolates Espresso Blend, Espresso Beans may contain undeclared almonds

 

Kent, Washington, 2017-Nov-15 — /EPR Retail News/ — Seattle Gourmet Foods of Kent, Washington is recalling 127 cases of Costco item # 2335, Dilettante Chocolates Espresso Blend, Espresso Beans in Semisweet, Milk and White Chocolate, because it may contain undeclared almonds.  People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume this product.

Dilettante Chocolates Espresso Blend was distributed to Costco Business Centers located in Lynnwood, Washington and Tukwila, Washington, and Costco Northwest located in Salt Lake City, Utah between August 22, 2017 and November 9, 2017.

The product is packaged in a clear plastic bag, net weight 5-pounds and has the UPC 37041 05211.  The affected product is labeled as Dilettante Chocolates Espresso Blend, Item# 2335, Lot Code 12287, and has the Best By 021619.

There have been no any illnesses or deaths reported to date in consumption of the recalled product. No other Dilettante packaged products are affected.

The recall was initiated after the firm discovered the chocolate covered almonds were mixed and packaged with the Dilettante Espresso Blend.  Product was distributed in packaging that did not reveal the presence of almonds.

Seattle Gourmet Foods is deeply sorry for the inconvenience this may have caused to our customers and has implemented a more standardized control of blending procedures to avoid errors like this in the future.

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

People who have an allergy or severe sensitivity to almonds should not consume the recalled product and should return Dilettante Chocolates Espresso Blend to the place of purchase for a full refund.  Consumers with questions may contact the company at 1-206-957-9834 from 5:00am to 3:30pm PST on Monday to Friday.

Consumers Contact:

 1-206-957-9834

Media Contact:

Laura Henry
laura@seattlegourmetfoods.com
206-957-9834

Source: FDA

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21st Century Snack Foods voluntarily recalls Dark Chocolate Almonds that may contain undeclared milk allergen

21st Century Snack Foods voluntarily recalls Dark Chocolate Almonds that may contain undeclared milk allergen

 

Ronkonkoma NY 11779, 2017-Nov-01 — /EPR Retail News/ — 21st Century Snack Foods, of Ronkonkoma NY 11779, is voluntarily issuing the following recall: Dark Chocolate Almonds: Packaged in a 6 oz peg / stand up bag.  UPC# 030603 228549. Affected Lot #’s are 16100 thru 17300. The product brand is 21st Century Snack Foods. The product is packaged in a plastic hanging / stand-up bag.

These products may contain an undeclared milk allergen. People who have an allergy or severe sensitivity to milk allergen run the risk of serious or life threatening allergic reaction if they consume these products.

No Illnesses have been reported to date.

This product may have been distributed to the following states, and they reached consumers through retail stores: AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WV, WI, WY

The recall was initiated after it was discovered, that the Dark Chocolate Almonds containing the milk allergen were distributed in packaging that did not reveal the presence of the milk allergen.

Consumers who have purchased this product will be asked to dispose of this product and contact the company directly via email for a full refund at centurysnack@gmail.com

Consumers with questions, may also contact the company at 631-588-8000 and ask to speak with the recall coordinator, Michael Bell. Hours of operation are 9:30 am – 3:30 pm

This product was manufactured by GKI Foods of Brighton, Michigan and packaged and distributed under the 21st Century Snack Foods Brand.

This recall is an extension of the GKI Foods LLC recall announced on October 27 2017

Consumers Contact:

Michael Bell
centurysnack@gmail.com
631-588-8000

Source: FDA

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Rucker’s Wholesale and Service Co voluntarily recalls Uncle Buck’s and Family Choice Dark Chocolate Peanuts due to undeclared milk

Rucker’s Wholesale and Service Co voluntarily recalls Uncle Buck’s and Family Choice Dark Chocolate Peanuts due to undeclared milk

 

Bridgeport, IL, 2017-Nov-01 — /EPR Retail News/ — Rucker’s Wholesale and Service Co of Bridgeport, IL is voluntarily recalling all of Uncle Buck’s and Family Choice Dark Chocolate Peanuts packaged in standup twist tie bag, due to the presence of an undeclared milk ingredient. People who have an allergy or sensitivity to milk run the risk of serious or life threatening allergic reaction if they consume this product. No illness associated with this recall has been reported.

The affected product is packaged in a 8.5oz clear twist tie bag with Uncle Buck’s and Family Choice label. Both brands are UPC 0 52545 10226 8. The recall product was sold between March 7, 2016 and October 30, 2017 and distributed nationwide.

The Uncle Bucks brand was distributed to Bass Pro Shops. The Family Choice brand was distributed to Bomgaars Supply, L&M Fleet Supply, North 40 Outfitters and Runnings.

The recall product was sold between March 7, 2016 and October 30, 2017.

The recall was initiated after Rucker’s received notification from our supplier GKI Foods of a recall due to undeclared milk allergen present in the dark chocolate. Consumers who have purchased any of these items are urged to destroy the product. Consumers with questions may contact Rucker’s at 618-945-2411, or 800-663-1857 Mon – Fri 7:30 am – 4:30 pm CST, or email – customerservice@ruckerscandy.com.

Consumers with an allergy to milk should not eat the product.

Consumers Contact:

Rucker’s
customerservice@ruckerscandy.com
618-945-2411
800-663-1857

Source: FDA

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Les Chateaux De France, Inc. recalls bacon-wrapped scallops due undeclared milk

WASHINGTON, 2017-Oct-19 — /EPR Retail News/ — Les Chateaux De France, Inc., an Inwood, N.Y. establishment, is recalling approximately 4,225 pounds of bacon-wrapped scallops due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (Oct. 18, 2017). The products contain milk, a known allergen, which was not declared on the product label.

The frozen, raw, marinated scallops wrapped in bacon were produced on various dates from April 19, 2016 through October 13, 2017. The following products are subject to recall: 

  • 3.5-lb. plastic-lined, boxed packages containing 100 pieces of “MARINATED SCALLOPS WRAPPED IN BACON SECURED WITH A TOOTHPICK.”

The products subject to recall bear establishment number “EST. 1393” inside the USDA mark of inspection. These items were shipped to institutional locations in Delaware, Florida, New Jersey, New York and Pennsylvania.

The problem was discovered on October 17, 2017 by an FSIS Enforcement, Investigations and Analysis Officer (EIAO) while conducting a Food Safety Assessment (FSA).

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 Jerry Shapiro, owner, at (516) 239-6795 or sales@leschateauxinfo.com.

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 10 a.m. to 6 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: https://www.fsis.usda.gov/reportproblem.

USDA Recall Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

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

Source: USDA

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Whole Foods Market voluntarily recalls 365 Everyday Value Organic Raisin Bran that contains undeclared peanuts

Whole Foods Market voluntarily recalls 365 Everyday Value Organic Raisin Bran that contains undeclared peanuts

 

Austin, Texas, United States, 2017-Oct-10 — /EPR Retail News/ — Whole Foods Market stores is voluntarily recalling 365 Everyday Value Organic Raisin Bran because the product contains undeclared peanuts that were not listed on the product label. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.

The affected product was sold in Whole Foods Market stores in the U.S. and online at Amazon.com. The product was packaged in 15 oz. boxes labeled 365 Everyday Value Organic Raisin Bran with UPC code 9948243903 and best-by date of June 4, 2018. The issue was discovered after Whole Foods Market determined the packaging contained Peanut Butter Cocoa Balls instead of Organic Raisin Bran. All affected product has been removed from store shelves and online. No reactions have been reported to date.

Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Customers who purchased the product online will receive additional information via email. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.

Consumers Contact:

1-844-936-8255

Media Contact:

Betsy.Harden@wholefoods.com
512.542.3198

Source: FDA

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TAI FOONG USA recalls Royal Asia Shrimp Wonton Noodle Soup that may contain undeclared egg

TAI FOONG USA recalls Royal Asia Shrimp Wonton Noodle Soup that may contain undeclared egg

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Seattle, WA, 2017-Oct-05 — /EPR Retail News/ — TAI FOONG USA of Seattle, WA is recalling Royal Asia Shrimp Wonton Noodle Soup, because it may contain undeclared egg.  People who have an allergy or severe sensitivity to egg or egg products run the risk of serious or life-threatening allergic reaction if they consume these products. Individuals who are not allergic to eggs may safely consume this product.

Product was distributed in Washington, Oregon, Montana, Idaho, Utah and Alaska and were purchased exclusively at Costco beginning January 2017.

Royal Asia Shrimp Wonton Noodle Soup; Net weight 3.94lb (1.79kg) 63oz; 6 bowl pack.  One allergic reaction complaint has been CONFIRMED to date. The recall was initiated after the product was tested for presence of egg, and was confirmed. Because the packaging does not reveal the presence of Egg the product was immediately pulled from the shelves at Costco and destroyed, all other product was identified and isolated in the cold storage facilities and placed on hold to be properly labeled.

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

Tai Foong USA is asking consumers to return product to the store where purchased to request a full refund if there is an allergy concern. Affected product should then be discarded in a secure place and not consumed.

For more information please visit www.northernchef.com or contact 800-388-3666 #200

Consumers Contact:

Bart Cox
800-388-3666 #200

Source: FDA

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Sid Wainer & Son® voluntarily recalls Jansal Valley® brand Dried Chili De Arbol Peppers due to undeclared peanuts

Sid Wainer & Son® voluntarily recalls Jansal Valley® brand Dried Chili De Arbol Peppers due to undeclared peanuts

 

New Bedford, MA, 2017-Oct-05 — /EPR Retail News/ — Sid Wainer & Son® of New Bedford, MA is voluntarily recalling Jansal Valley® brand Dried Chili De Arbol Peppers because it does not have the proper allergens identified, being peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.

The product is packaged in a clear plastic clamshell container labeled as Jansal Valley® Dried Chili De Arbol Peppers, packaged in 1 ounce sizes. The cases contain 12 1 oz units each.

Product best by dates include 9/11/2018, 9/22/2018 and 9/26/2018.

Dried Chili De Arbol Peppers were distributed Nationwide in retail stores and grocery chains.

No illnesses have been reported to date in connection with this problem.

During repacking, the peanut contamination was discovered in the sealed bulk containers of the product.

Consumers who have purchased 1 ounce packages of Jansal Valley® Dried Chili De Arbol Peppers, please destroy the above mentioned product if your company is in possession of it.

Consumers with questions may contact the company at 1-800-423-8333 at extension 168 or 119 between the hours of 9:00 am and 5:00 pm.

About Sid Wainer & Son®: Sid Wainer & Son®, based in New Bedford, MA, has been the most prominent importer and distributor of specialty produce in the country since 1914. In addition to produce, Sid Wainer & Son® offers artisanal cheese and specialty foods, including their exclusive Jansal Valley® Line. Sid Wainer & Son® suppliers over 30,000 of the finest restaurants, hotels, gourmet shops, retailers, and caterers both domestically and internationally. To learn more about Sid Wainer & Son, visit www.Sidwainer.com.

Consumers Contact:

1-800-423-8333

Media Contact:

Gary Marcotte
gmarcotte@SidWainer.com
(800) 423-8333 x 340

Source: FDA

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USDA FSIS: Belmont Sausage recalls smoked turkey products due to undeclared milk

WASHINGTON, 2017-Oct-03 — /EPR Retail News/ — Belmont Sausage Co., an Elk Grove Village, Ill. establishment, is recalling an undetermined amount of smoked turkey products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products contain milk, a known allergen, which is not declared on the product label.

The smoked turkey drumstick items were produced from September 27, 2015 through September 27, 2017. The following products are subject to recall: [View Labels (PDF Only)]

  • 25- to 29-oz. plastic-lined, boxed packages containing 18 pieces of “Wolverine Packing Co. complete protein solutions Smoked Turkey Drumsticks” with lot code 20144.
  • 20- to 24-oz. plastic-lined, boxed packages containing 20 pieces of “Wolverine Packing Co. complete protein solutions Smoked Turkey Drumsticks” with lot code 20148.

The products subject to recall bear establishment number “P-21309” inside the USDA mark of inspection. These items were shipped to an institutional location in Michigan that further distributed nationwide.

The problem was discovered by FSIS Inspection Program Personnel while performing routine label verification checks.

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 or media with questions about the recall can contact Michael Mulica, Co-President, at (847) 302-8011 or mike@belmontsausage.com.

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 10 a.m. to 6 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: https://www.fsis.usda.gov/reportproblem.

USDA Recall Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

SOURCE: USDA FSIS

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

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Wakefern Food recalls its ShopRite Semi-Sweet Real Chocolate Chips due to undeclared milk

Wakefern Food recalls its ShopRite Semi-Sweet Real Chocolate Chips due to undeclared milk

Silver Spring, MD, 2017-Sep-06 — /EPR Retail News/ — Wakefern Food Corp. has initiated a voluntary recall of its ShopRite brand Semi-Sweet Real Chocolate Chips. The chips were sold in 24 oz. bags bearing a UPC bar code of 041190 02668 and Best if Used By dates of April 11, 2019 and April 12, 2019.

The recall was issued because the package may contain milk chocolate chips, and milk is not declared in the ingredient statement. No illnesses have been reported but people who are allergic to milk could experience an allergic reaction if they consume the chips. No other package sizes or date codes are being recalled.

“Customers who purchased the chocolate chips may return them for an immediate refund or replacement,” said Karen Meleta, vice president of Consumer and Corporate Communications for Wakefern. “People who are not allergic to milk and those who are not concerned about consuming dairy ingredients may choose not to return the product as it is otherwise safe to eat,” she added.

The product was sold in ShopRite, The Fresh Grocer and other retail stores located throughout the Northeast. Wakefern has contacted ShopRite and The Fresh Grocer Price Plus Club customers who have purchased this product to alert them to the recall.

Customer questions or concerns about the recall can be directed to 1-800-ShopRite (1-800-746-7748) Monday – Friday from 8 a.m. to 6 p.m. and from 9 a.m. to 5 p.m. on Saturday and Sunday.

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About Wakefern Food Corp.

From a small, local cooperative that began with eight grocery store owners, Wakefern Food Corp. has grown into the largest retailer-owned cooperative in the United States. Founded in 1946, the cooperative comprises 50 members who today independently own and operate 343 supermarkets under the ShopRite, The Fresh Grocer, Price Rite and Dearborn Market banners in New Jersey, New York, Connecticut, Pennsylvania, Maryland, Delaware, Massachusetts, Rhode Island and Virginia. Together with its member companies, Wakefern employs more than 70,000 people, and is one of the largest employers in New Jersey. For more information, please visit www.wakefern.comdisclaimer icon

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Consumers

1-800-ShopRite (1-800-746-7748)

Media

Maureen Gillespie
 maureen.gillespie@wakefern.com
(732) 906-5295

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Dedinas Franzak Enterprises recalls several brands of butter flavored popcorn that may contain undeclared milk

Grand Rapids MI, 2017-Aug-31 — /EPR Retail News/ — Dedinas Franzak Enterprises of Grand Rapids MI, is recalling several brands of butter flavored popcorn because they may contain undeclared milk. People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled butter flavored popcorn brands are:

30NOV2017 – UPC 614156061992 distributed in Michigan. Gourmet Select 12oz 24NOV2017 – UPC 899788002432 distributed in Wisconsin. Gold Emblem 5oz 24NOV2017, 01DEC2017 and 30DEC2017 – UPC 05042844879 distributed in California, Indiana, Virginia, Pennsylvania, Texas, Alabama, New Jersey, South Carolina, and Florida retail stores. Spartan 8oz 01SEP2017 – UPC 011213027395 distributed in Michigan.

The product comes in a Poly and/or poly metalized film package marked with lot codes on the top right front panel.

No illnesses have been reported to date in connection with this problem.

The recall was initiated after a non-illness consumer complaint in relation to flavor.

Consumers who have purchased any of the above products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-616-784-6095 EXT 22.

Link to the Initial Recall.

Consumers Contact:

mballard@cksnacks.com
616-784-6095, Ext. 22

Source: FDA

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Rajbhog Distributors GA. Inc. recalls Jalebi that may contain undeclared Almond

Rajbhog Distributors GA. Inc. recalls Jalebi that may contain undeclared Almond

 

Duluth, GA., 2017-Aug-31 — /EPR Retail News/ — Rajbhog Distributors GA. Inc. of Tucker GA-30084 is recalling 1467  packets of Jalebi because it may contain undeclared Almond pcs. People who have an allergy or severe sensitivity to Almonds run the risk of serious or life- threatening allergic reaction if they consume these products.

These Jalebi packets (Code number-P026 and P027) were distributed to the grocery stores located in Georgia, South Carolina, North Carolina, Florida, Mississippi, and Tennessee. It might have reached the consumers through retail stores.

These products can be identified by visibly looking at the Jalebi packets packed in clear containers as Almonds are used as a toppings to garnish the Indian sweet, Jalebi.

As of today, there has not been single complaint reported.

This problem was highlighted by FDA inspectors while inspecting our food distribution facility. The problem was caused due to recent change in the packing of the product to enhance the appearance of the product.

The consumers who have purchased clear containers of Rajbhog brand Jalebi are urged to return to the place of purchase for a full refund.

The consumers with questions may contact the above company at (678) 924-1440 from Monday to Friday 10:00 AM to 6:00 PM.

Consumers Contact:

(678) 924-1440

Media Contact:

Rupesh Bhatt
(678) 924-1440
Fax – (678) 924-1441

Source: FDA

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Dedinas-Franzak Enterprises recalls Big Win, Butter Popcorn that may contain undeclared milk

Grand Rapids, Michigan, 2017-Aug-29 — /EPR Retail News/ — Dedinas-Franzak Enterprises is recalling Big Win, Butter Popcorn Artificially Flavored 5 OZ, UPC #0-11822-58492-0, This product is artificially flavored and milk is not specifically called out in the Allergen Statement. The product may contain milk and people who have an allergy or severe sensitivity to Milk may run the risk of serious or life-threatening allergic reaction if they consume this product. The concern was identified through a non-illness consumer complaint in relation to flavor.

Approximately 3,000 units of Big Win, Butter Popcorn Artificially Flavored product were distributed throughout the Rite Aid chain; this product is sold in the snack aisle. Product Expiration Dates included in the recall are the following: 16 FEB 2018. These date codes can be found in black ink printed on the front top right of the package.

There have been no injuries or illnesses reported to date associated with this product.

Customers who purchased the recalled product should return it to the point of purchase for a full refund. Consumers with questions may contact: Dedinas-Franzak Enterprises, 616-784-6095 extension 22 Monday through Friday 8AM to 4PM EST. Via email at mballard@cksnacks.com.

Consumers Contact:

mballard@cksnacks.com
616-784-6095

Source: FDA

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Luvo Inc. (USA) recalls poultry products mislabeled as Chicken Chile Verde but contain Turkey Meatloaf

WASHINGTON, 2017-Aug-15 — /EPR Retail News/ — Luvo Inc. (USA), a Blaine, Wash. establishment, is recalling approximately 4,805 pounds of poultry products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (Aug. 12, 2017). The products are mislabeled as Chicken Chile Verde that contain milk and soy, but contain Turkey Meatloaf, which has additional allergens, eggs and fish (anchovies), that are not declared on the product label.

The products were produced on June 13, 2017. The following product is subject to recall: 

  • 10 oz. retail cartons containing “LUVO Steam in Pouch A LITTLE SPICE CHICKEN CHILE VERDE with white chicken, black beans, and polenta” and lot code: 2018 JUN13 A, with a best before date of June 13, 2018.

The products subject to recall bear establishment number “424” inside the Canadian Food Inspection Agency (CFIA) mark of inspection. These items were shipped to distributors in California, Florida, Indiana, Iowa, Missouri, North Carolina, Ohio, Pennsylvania, Texas, Virginia and Wisconsin for further distribution.

The problem was discovered after the firm received consumer complaints of the wrong meal inside the retail boxes.

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 will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers with questions about the recall can contact the Digital Community Manager Oli Maughan, Luvo, Inc., at (844) 880-5866. Media with questions about the recall can contact Oli Maughan, Luvo, Inc. by phone at (604) 340-1166 or e-mail omaughan@luvoinc.com.

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 10 a.m. to 6 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 Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

Contact:
Congressional and Public Affairs
Jennifer Dallis
(202) 720-9113
Press@fsis.usda.gov

Source: USDA

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USDA FSIS: Kenosha Beef International recalls beef patty products due to misbranding and an undeclared allergen

USDA FSIS: Kenosha Beef International recalls beef patty products due to misbranding and an undeclared allergen

 

WASHINGTON, 2017-Aug-10 — /EPR Retail News/ — Kenosha Beef International, LTD., a Kenosha, Wis. establishment, is recalling approximately 3,960 pounds of beef patty products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (Aug. 9, 2017). The products may contain milk, in the form of cheddar cheese, a known allergen that was not declared on the finished product label. The products also contain undeclared bacon.

The bacon cheddar beef patty products were produced on June 14, 2017. The following products are subject to recall: 

  • 4-lb retail carton containing 12, 1/3 pound burgers of “JP O’REILLY’S, PUB BURGER, FAMILY PACK, MADE FROM BEEF CHUCK,” with a sell-by date of 01-10-18.
  • 24-lb cases of “JP O’REILLY’S, BACON & CHEDDAR BEEF PATTIES” with sell-by date of 01-10-18 and case codes of 0614KS42065, 0614KS42066, 0614KS42067, 0614KS42068 and 0614KS42070.

The products subject to recall have establishment number “EST. 425B” printed adjacent to the sell-by date on the retail carton and inside the USDA mark of inspection on the shipping case. These items were shipped to retail locations in Connecticut, Delaware, Maryland, New Jersey, New York and Pennsylvania.

The problem was discovered on Aug. 9, 2017 when the firm received two consumer complaints regarding the bacon cheddar beef patties not being labeled as bacon and cheddar. Specifically, the products were labeled as “JP O’Reilly’s PUB BURGER,” but contained “JP O’Reilly’s Bacon Cheddar Beef Patties.”

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 Peter Policastro, President, at (732) 515-9314. Members of the media with questions about the recall can contact Dennis Vignieri, CEO, at (262) 859-2272 ext. 1205.

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 10 a.m. to 6 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 Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

Contact:

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

Source: USDA

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Meijer voluntarily recalls its Wave Zone One Piece Zip Infant Swimsuits due to possible choking hazard

GRAND RAPIDS, Mich., 2017-Aug-09 — /EPR Retail News/ — Meijer is announcing a voluntary recall of its Wave Zone One Piece Zip Infant Swimsuits produced and sold exclusively at Meijer. Meijer recently recalled approximately 22,246 of the Wave Zone One-Piece Zip Swimsuits because the snaps on the bottom of the suit can detach and pose a choking hazard.

The swimsuit sold for $14 between January 1, 2017 and July 17, 2017. There have been no known injuries reported. Meijer is recalling the product as a precautionary measure.

The newborn, infant and toddler swimsuit has a zipper on the back and four snaps on the bottom. The swimsuit sold in the following four color styles: blue and gray with a shark; white and navy stripes with anchor pattern; pink and teal with a strawberry; pink and white with a fish pattern. The styles were available in the following sizes: 0-3m, 3-6m, 6-9m, 12m, 18m, and 24m. “Wave Zone” and “Made in China” are printed on the inner collar. The tracking number located on the sewn-in label on the inner side seam is “NOV 2016 021-14328.”

Customers should stop using swimsuit and return it to the customer service desk at any Meijer store for a full refund. For additional information, please contact Meijer at (800) 543-3704, available 24 hours a day, seven days a week. Meijer stores are also opened 24 hours a day, seven days a week.

About Meijer:

Meijer is a Grand Rapids, Mich.-based retailer that operates more than 230 supercenters and grocery stores throughout Michigan, Ohio, Indiana, Illinois, Kentucky and Wisconsin. A privately-owned and family-operated company since 1934, Meijer pioneered the “one-stop shopping” concept and has evolved through the years to include expanded fresh produce and meat departments, as well as pharmacies, comprehensive apparel departments, pet departments, garden centers, toys and  electronics. For additional information on Meijer, please visit www.meijer.com. Follow Meijer on Twitter @twitter.com/.

Contact:
Frank Guglielmi
616-791-3814
frank.guglielmi@meijer.com

Source: Meijer

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USDA FSIS: Good Food Concepts, LLC. recalls beef products that may be contaminated with E. coli O26

WASHINGTON, 2017-Aug-09 — /EPR Retail News/ — Good Food Concepts, LLC., a Colorado Springs, Colo. establishment, is recalling approximately 1,290 pounds of raw intact and non-intact beef because the products may be contaminated with E. coli O26, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (Aug. 7, 2017).

The raw intact and non-intact beef items were processed and packaged on Aug. 3 and Aug. 4, 2017. The following products are subject to recall:

  • Various weights of individual packages of “CALLICRATE BEEF, Celebrate goodness, Celebrate life, Filet Mignon,” with lot code 170731CC.
  • Various weights of individual packages of “CALLICRATE BEEF, Celebrate goodness, Celebrate life, Brisket Flat,” with lot code 170731CC.
  • Various weights of individual packages of “CALLICRATE BEEF, Celebrate goodness, Celebrate life, Sirloin Tip,” with lot code 170731CC.
  • Various weights of individual packages of “CALLICRATE BEEF, Celebrate goodness, Celebrate life, Ribeye,” with lot code 170731CC.
  • Various weights of individual packages of “CALLICRATE BEEF, Celebrate goodness, Celebrate life, Stew Meat,” with lot code 170731CC.
  • Various weights of individual packages of “CALLICRATE BEEF, Celebrate goodness, Celebrate life, New York Strip,” with lot code 170731CC.
  • Various weights of individual packages of “CALLICRATE BEEF, Celebrate goodness, Celebrate life, Skirt Steak,” with lot code 170731CC.
  • Various weights of individual packages of “CALLICRATE BEEF, Celebrate goodness, Celebrate life, Top Sirloin,” with lot code 170731CC.
  • Cases of 14.60-lb of “RANCH FOODS DIRECT GROUND BEEF 80/20 BEEF,” with lot code 170804.
  • Cases of 6.40-lb of “RANCH FOODS DIRECT GROUND BEEF 80/20” BEEF, with lot code 170803.
  • Cases of 6.40-lb of “RANCH FOODS DIRECT PHILLY MEAT BEEF,” with lot code 170803.
  • Cases of 6.40-lb of “RANCH FOODS DIRECT TOP SIRLOIN STEAK 8oz BEEF,” with lot code 170803.
  • Cases of 40-lb of “RANCH FOODS DIRECT GROUND CHUCK BEEF,” with lot code 170804.
  • Cases of 6.40-lb of “RANCH FOODS DIRECT GROUND BEEF (73/27),” with lot code 170803.
  • Cases of 40-lb of “RANCH FOODS DIRECT FLAT IRON BEEF,” with lot code 170804.
  • Cases of “FAMILY BUNDLE, 4-GROUND BEEF 80% LEAN 20% FAT, 1-LONDON BROIL, 2-PKGS CUBE STEAKS, 6-FLATIRON STEAKS, $91.99” with lot code 170804.
  • Cases of “STEAK BUNDLE, 4-RIBEYE STEAKS, 4-NEW YORK STRIP STEAKS, 4-TOP SIRLOIN STEAKS, 4-FILET MIGNON $174.99” with lot code 170804.
  • Cases of “RIBEYE STEAK BUNDLE, 10-RIBEYE STEAKS, $117.99” with lot code 170803.
  • Cases of “COLORADO BUNDLE, 4-SKIRTS STEAKS, 4-CHUCK EYE STEAKS, 4-TOP SIRLOIN, 2-CHUCK ROAST, 15-GROUND BEEF 80% LEAN 20%FAT, $199.19” with lot code 170804.
  • Cases of 20-lb of “GROUND BEED, 90% LEAN, 10% FAT $125.99” with lot code 170804.
  • Packages of “ALL NATURAL CALLIGRATE BEEF, Celebrate goodness, Celebrate Life, GROUND BEEF.”

The products subject to recall bear establishment number “EST. 27316” inside the USDA mark of inspection. These items were shipped to retail locations, wholesale locations, and restaurants in Colorado Springs, Colorado.

The problem was discovered on Aug. 5, 2017 when plant management at Good Food Concepts, LLC notified FSIS in-plant inspection personnel that they tested a production lot of carcasses they received from the Callicrate Ranch on July 31, 2017. The carcass trimmings from the N60 analysis was positive for non-O157 STEC serogroup O26.

Many clinical laboratories do not test for non-O157 Shiga toxin-producing E. coli (STEC), such as STEC O26 because it is harder to identify than STEC O157. People can become ill from STECs 2–8 days (average of 3–4 days) after consuming the organism. Most people infected with STEC O26 develop diarrhea (often bloody), and vomiting. Some illnesses last longer and can be more severe. Infection is usually diagnosed by testing of a stool sample. Vigorous rehydration and other supportive care is the usual treatment; antibiotic treatment is generally not recommended.

Most people recover within a week, but, rarely, some develop a more severe infection. Hemolytic uremic syndrome (HUS) is uncommon with STEC O26 infection. HUS can occur in people of any age but is most common in children under 5 years old, older adults and persons with weakened immune systems. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.

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 Dave Anderson, Operations Manager, at (719) 473-2306.

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 10 a.m. to 6 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.

PREPARING PRODUCT FOR SAFE CONSUMPTION
USDA Meat and Poultry Hotline
1-888-MPHOTLINE or visit www.fsis.usda.gov
Wash hands with warm, soapy water for at least 20 seconds before and after handling raw meat and poultry. Wash cutting boards, dishes and utensils with hot, soapy water. Immediately clean spills.Keep raw meat, fish and poultry away from other food that will not be cooked. Use separate cutting boards for raw meat, poultry and egg products and cooked foods.

Color is NOT a reliable indicator that meat has been cooked to a temperature high enough to kill harmful bacteria.

The only way to be sure the meat or poultry is cooked to a high enough temperature to kill harmful bacteria is to use a thermometer to measure the internal temperature.

  • Fish: 145°F
  • Beef, pork, lamb chops/steaks/roasts: 145°F with a three minute rest time
  • Ground meat: 160°F
  • Poultry: 165°F
  • Hot dogs: 165°F or steaming hot

Refrigerate raw meat and poultry within two hours after purchase or one hour if temperatures exceed 90º F. Refrigerate cooked meat and poultry within two hours after cooking.

 

USDA Recall Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

Contact:
Congressional and Public Affairs
Veronika Medina
(202) 720-9113
Press@fsis.usda.gov

Source: USDA

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Hahn Brothers, Inc. recalls ready-to-eat ham products due to misbranding and an undeclared malted barley

WASHINGTON, 2017-Aug-07 — /EPR Retail News/ — Hahn Brothers, Inc., a Westminster, Md. establishment, is recalling approximately 115,773 pounds of ready-to-eat (RTE) ham products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (Aug. 5, 2017). The products contain malted barley, a known allergen, which is not declared on the final product label.

The ready-to-eat ham products were produced from Dec. 17, 2015 to July 27, 2017. The products have a 70-day sell-by date. The following product is subject to recall: 

  • 1.75-lb. of vacuum-packed mini ham packages containing “Lou’s Garrett Valley Natural, All Natural black forest seasoned uncured ham nugget, FULLY COOKED WOOD SMOKED” with a case code 74045.

The products subject to recall bear establishment number “EST. 2000” inside the USDA mark of inspection. These items were shipped to a distributor in New Jersey and further distributed to retail locations.

The problem was discovered when the FSIS Office of Public Health Science (OPHS) received a consumer complaint on July 11, 2017 with regard to a mislabeling of Lou’s Garret Valley Black Forest Seasoned Uncured Ham Nugget produced by Hahn Brothers Incorporated. The complainant noted that malted barley is listed as an ingredient on the company’s website, but is not listed as an ingredient on the product label.

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.

Media and consumers with questions about the recall can contact Barry Blevins, Vice President of Operations, at (443) 375-7762.

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 10 a.m. to 6 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: https://www.fsis.usda.gov/reportproblem.

USDA Recall Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

Contact:
Congressional and Public Affairs
Veronika Medina
(202) 720-9113
Press@fsis.usda.gov

Source: USDA

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Fairway “Like No Other Market”® recalls Fairway brand Cookies Blondie that may contain undeclared ingredient

Fairway “Like No Other Market”® recalls Fairway brand Cookies Blondie that may contain undeclared ingredient

 

New York, NY, 2017-Aug-04 — /EPR Retail News/ — Fairway ‘‘Like No Other Market’’ ® of New York, NY Is voluntarily recalling Fairway brand Cookies Blondie, because the product may contain undeclared ingredient, walnuts. People who have an allergy or severe sensitivity to nuts run the risk of serious or life-threatening allergic reaction if they consume this product.

The Fairway brand Cookies Blondie were distributed to Fairway stores in New York, New Jersey and Connecticut and also through home delivery programs provided by Fairway E-commerce,
Google and Instacart.

The product is packaged in octagon-shaped plastic containers that are black on the bottom and clear on the top with a standard weight of 10 oz.  The product bears either Item Code 268492 XXXXXX or 263413 XXXXXX.  All ‘‘SELL BY’’ Date codes are being recalled. No other Fairway products are involved.

The recall is the result of a discovery by Fairway personnel. The company has ceased distribution of the Fairway brand Cookie Blondie and removed the product from Fairway store shelves.

Consumers who purchased the affected Fairway brand Cookies Blondie should return the product to the place of purchase for a full refund. Consumers with questions may contact the company at (646)616-8265, Monday  Friday, 9 am  5 pm EST.

Consumers Contact:

(646)616-8265

Source: FDA

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Cesina Sausage Company recalls not-ready-to-eat pork sausage product labeled ready-to-eat

WASHINGTON, 2017-Jul-22 — /EPR Retail News/ — Cesina Sausage Company, an Aliquippa, Penn. establishment, is recalling approximately 10 pounds of pork sausage product due to misbranding, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (July 20, 2017). The product label identifies this product as ready-to-eat (RTE), when in fact this product is not-ready-to-eat (NRTE).

The pork kolbassi (sausage) item was produced on June 22, 2017. The following product is subject to recall: 

  • 1-lb. vacuumed packed packages of “CESINA’S BRAND FULLY COOKED • SMOKED PORK KOLBASSI”.

The products subject to recall bear establishment number “EST. 5073” inside the USDA mark of inspection. This item was shipped to a local grocery store in Aliquippa, Pennsylvania.

The problem was discovered when a retail customer noticed that the product label was incorrect.

There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumers who have purchased this product are urged not to consume it. This product 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 William Costanza, Owner, at (724) 375-2450.

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 10 a.m. to 6 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 Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

Contact:
Congressional and Public Affairs
Gabrielle N. Johnston
(202) 720-9113
Press@fsis.usda.gov

Source: USDA

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Garden of Light, Inc. recalls Woodstock Organic Matcha Vanilla Oats that may be contaminated with Listeria monocytogenes

Garden of Light, Inc. recalls Woodstock Organic Matcha Vanilla Oats that may be contaminated with Listeria monocytogenes

 

East Hartford, CT, 2017-Jul-19 — /EPR Retail News/ — Garden of Light, Inc. dba Gluten Free Solutions of East Hartford, CT, is voluntarily recalling the Woodstock Organic Matcha Vanilla Oats, 1.8 oz. which is manufactured by Garden of Light for Blue Marble Brands. The product 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. The recalled item, Woodstock Organic Matcha Vanilla Oats, was distributed nationwide in retail stores.

The product comes in a 1.8 oz. paperboard cup with a green laminated film lid. The UPC Code is 0-42563-01786-6. The product is marked with the Best Buy Date Code of “SELL BY MAY 11 2018” on the bottom of cup.

A second lot with the Best Buy Date Code of “SELL BY JUNE 23 2018” was intercepted before released to the general public.

The potential for contamination was noted after the ingredient supplier, Hudson Valley Farms( HVF), Inc. notified Garden of Light, Inc. of potential contamination of one of the ingredients. The potential contaminated ingredient was thoroughly tested and was negative for Listeria. No illnesses have been reported to date in connection with this problem, however, out of an abundance of caution, Garden of Light, Inc., notified Blue Marble and is recalling the Woodstock Organic Matcha Vanilla Oats. The production of the product has been suspended while the company continues to investigate the source of the problem.

Consumers who have purchased 1.8 oz. cups are urged to destroy the product and bring the purchase receipt to the place of purchase for a full refund. Consumers with questions may contact Blue Marble Brands at (888) 534-0246, M – F between 9 am and 5 pm, or at www.woodstock-foods.com.

Consumers Contact:

Blue Marble Brands
 (888) 534-0246

Source: FDA

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Texas Legend Foods recalls its Silver Star Chipotle Queso Dip due to undeclared cheese, milk and eggs

Austin, TX, 2017-Jul-17 — /EPR Retail News/ — Texas Legend Foods of Austin, TX, is recalling its 16 ounce jars of Silver Star Chipotle Queso Dip because they contain undeclared cheese, milk and eggs. People who have allergies to cheese, milk and eggs run the risk of a serious or life-threatening allergic reaction if they consume this product.

The recalled “Silver Star Chipotle Queso Dip” was distributed nationwide in retail stores.

The product comes in a 16 ounce clear glass jar marked with one of the following Lot #’s: 060AFV7A, 072AFV7A, 072AFV7B, 090AFV7A, 111AFV7A which is stamped on the top of the glass jar beneath the lid. UPC CODE #819993005394

No illnesses have been reported to date in connection with this problem.

The recall was initiated after it was discovered that the milk, cheese and egg containing product was distributed in packaging that did not reveal the presence of the milk, cheese and egg. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company’s production and packaging processes.

Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.

Consumers who have purchased jars of “Silver Star Chipotle Queso Dip” are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 512-461-0269 between 9 am-5 pm CST or email natalie@texaslegendfoods.com. Information may also be found on our website at www.silverstarsalsa.com

Consumers Contact:

Natalie Jardine
natalie@texaslegendfoods.com
512-461-0269

Source: FDA

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Sunneen Health Foods recalls mislabeled Whole Foods Market PB&J parfaits

Sunneen Health Foods recalls mislabeled Whole Foods Market PB&J parfaits

 

Allentown, Pennsylvania, 2017-Jul-15 — /EPR Retail News/ — Sunneen Health Foods is voluntarily recalling mislabeled Whole Foods Market PB&J parfaits sold at five Whole Foods Market stores in New York and New Jersey because the products contained soy and tree nut (almond and coconut) allergens that were not listed on the product label. People who have an allergy or severe sensitivity to soy or tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.

No allergic reactions have been reported to date. All affected products have been removed from store shelves.

The products were sold in 8 oz. containers labeled as Whole Foods Market PB&J Parfaits. They can be identified by UPC codes 636910500448 and best-by dates before 7/13/2017. They were sold at the following Whole Foods Market stores:

  • 905 River Rd, Edgewater, NJ
  • 4 Union Square South, New York, NY
  • 238 Bedford Ave, Brooklyn, NY
  • 1095 6th Ave, New York, NY
  • 113 Route 9 S, Englishtown, NJ

Customers who purchased these product and wish to return them can bring a valid receipt into stores for a full refund. Consumers with additional questions should call Sunneen Health Foods’ customer service at 610 774-9894 between the hours of 8 am and 3 pm EST, Monday through Friday.

Consumers Contact:

610 774-9894

Source: FDA

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Coborn’s, Inc. recalls Gluten Free Chocolate Chip Bars that were incorrectly labeled as Gluten Free Fudge Brownies

St. Cloud, Minn., 2017-Jul-11 — /EPR Retail News/ — Coborn’s, Inc. of St. Cloud, Minn. is recalling packages of its Gluten Free Chocolate Chip Bars, some of which were incorrectly labeled as Gluten Free Fudge Brownies. The Gluten Free Fudge Brownie label does not indicate the product contains milk, however the Gluten Free Chocolate Chip Bars that are incorrectly labeled as Gluten Free Fudge Brownies do contain milk. People who have allergies to milk run the risk of a serious or life-threatening allergic reaction if they consume these products.

The recalled products were distributed and sold at Coborn’s and Cash Wise stores in Minnesota, North Dakota and South Dakota, as well as Marketplace Foods stores in Wisconsin, and Coborn’s Delivers in the Twin Cities Metro area. An internal review found a limited number of packages were sold. These products were sold between July 4, 2017 and July 6, 2017 and list an expiration date of July 10, 2017. Products with an expiration date of July 10, 2017 are the only products affected. The UPC is 7-33147-20522-8. Guests who are allergic to milk should destroy this product or return it to the store where it was purchased for a full refund.

No illnesses have been reported to date in connection with this problem.

The recall was initiated July 6 after it was discovered the Gluten Free Chocolate Chip Brownies were incorrectly labeled with a Gluten Free Brownie label. The problem has since been corrected and all packages going forward will contain the correct label.

Consumers with questions may contain the MORE Rewards Helpline at 1-844-700-MORE (6673).

Consumers Contact:

1-844-700-MORE (6673)

Source: FDA

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Raja Foods LLC recalls “ANARKALI PESHAWARI NAAN bread” because they may contain undeclared MILK

Raja Foods LLC recalls “ANARKALI PESHAWARI NAAN bread” because they may contain undeclared MILK

 

Skokie, IL, 2017-Jul-06 — /EPR Retail News/ — Raja Foods LLC of Skokie, Il is recalling its 15 ounce package of “ANARKALI PESHAWARI NAAN” because they may contain undeclared MILK. People who have allergies to MILK run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled “ANARKALI PESHAWARI NAAN” were distributed nationwide in retail stores.

The product comes in a 15 ounce plastic package marked “ANARKALI PESHAWARI NAAN” on the front of the bag. The manufacturing date and expiry date are on the back side of the bag. The dates are ink jetted and formatted as Year/Month/Date.

One illness has been reported to date in connection with this problem. The complaint occurred in New Jersey and was reported to us through the United States Food and Drug Administration (FDA.) The recall was initiated after it was discovered that the MILK containing product was distributed in packaging that did not reveal the presence of MILK. We are working with our supplier to change the labeling of the product going forward.

Consumers who have purchased “ANARKALI NAAN” are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-800-7923 EXT 2865, Monday to Friday 9am to 4pm CST.

Consumers Contact:

1-800-800-7923 EXT 2865

Media Contact:

Sam Patel
800-800-7923

Source: FDA

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Willow Tree Poultry Farm recalls tuna salad products mislabeled as chicken salad product

WASHINGTON, 2017-Jul-04 — /EPR Retail News/ — Willow Tree Poultry Farm, an Attleboro, Mass., establishment, is recalling approximately 440 pounds of tuna salad products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today (July 1, 2017). The product contains tuna, a known allergen which is not declared on the product label and the packing was mislabeled as chicken salad product.

The buffalo style chicken products were produced on June 27, 2017. The following products are subject to recall:

  • 12.5 oz. individual plastic containers of “buffalo style chicken salad.”

The products subject to recall bear establishment number “P-8827” inside the USDA mark of inspection. These items were shipped to Whole Foods Market locations in Connecticut, New Jersey and New York.

The problem was discovered by Whole Foods Market employees whilst unpacking the product.

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 Alex Cekala, General Manager, at (508) 951-8351. Media with questions about the recall can contact Walter Cekala, President, at (508) 944-0529.

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 10 a.m. to 6 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: https://www.fsis.usda.gov/reportproblem.

USDA Recall Classifications
Class I This 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 II This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.
Class III This is a situation where the use of the product will not cause adverse health consequences.

Contact:
Congressional and Public Affairs
Julie Schwartz
(202) 720-9113
Press@fsis.usda.gov

Source: USDA

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Dierbergs recalls various Deli Products due to undeclared fish and undeclared milk

Dierbergs recalls various Deli Products due to undeclared fish and undeclared milk

 

St Louis, 2017-Jul-03 — /EPR Retail News/ — Dierbergs is recalling various Deli Products with multiple use by dates in all retail stores because undeclared fish (anchovy) in a Caesar dressing and undeclared milk in 2 Santa Fe wraps. People who have allergies to fish and dairy run the risk of serious or life-threatening allergic reaction if they consume these products.

All of the packages have been removed from store shelves. No illnesses have been reported to date in connection with this problem. Product was distributed to all Dierbergs Markets retail locations in eastern and central Missouri and western Illinois.

All ‘Use By’ dates of the following products are included in this recall:

# Retail Products Reason for recall USE-BY-DATE
Grilled Chicken Caesar Wrap 10oz Undeclared Fish
Misbranded; Caesar Dressing has the incorrect ingredients listed		 7/2/17 and earlier
Grilled Chicken Caesar Salad 14oz Undeclared Fish
Anchovies are listed but fish is not declared as an allergen		 7/1/17 and earlier
Grilled Chicken Caesar Salad 8.5oz Undeclared Fish
Anchovies are listed but fish is not declared as an allergen		 7/1/17 and earlier
Classic Pinwheel Appetizer Wrap Platter 12ct Undeclared Fish
Misbranding;  Caesar Dressing has the incorrect ingredients listed		 7/2/17 and earlier
Santa Fe Grilled Chicken Wrap 11oz Undeclared Dairy
Misbranding;  Chicken (contains a dairy based additive) and cheese  are not listed as an ingredient on the label		 7/2/17 and earlier
Santa Fe Grilled Veggie Wrap 12oz Undeclared Dairy
Misbranding;  Cheese (contains dairy) is not listed as an ingredient on the label		 7/2/17 and earlier

The recall was initiated after it was discovered the fish containing (Caesar Dressing) and Dairy containing (Wraps) product was distributed in packages that did not reveal the presence of fish and milk respectively. Subsequent investigation indicated the omissions were the result of ingredient changes in the products. Production of the named products is suspended until FDA and Dierbergs are certain the labeling has been corrected. No other Dierbergs Markets branded products are affected by this recall. To date, Dierbergs Markets have received no reports of illnesses or allergic reactions associated with the recalled products.

Dierbergs Markets is asking consumers who have packages of the product to return them unopened to the place of purchase for a full refund. Consumers with questions may contact Dierbergs Markets at 1636-532-8884 Monday through Friday, 8 am to 4:30 pm CDT.

Consumers Contact:
Dierbergs Markets
636-532-8884

Media Contact:
Todd Vasel
636-812-1323

Source: FDA

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