New #foodsafety #recall #undeclared #milk #allergen in 18,570 lbs of chicken salad

Aldon Food Corp. Recalls Chicken Salad Products Due to Misbranding and Undeclared Allergens

Class I Recall062-2017
Health Risk: HighJun 8, 2017
Congressional and Public Affairs
Benjamin Bell
(202) 720-9113
Press@fsis.usda.gov
WASHINGTON, June 8, 2017 – Aldon Food Corporation, a Schwenksville, Pa. establishment, is recalling approximately 18,570 pounds of chicken salad 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 chicken salad products were produced from January 1, 2017 through May 31, 2017. The following products are subject to recall: [View Labels (PDF only)]
  • 5-lb. plastic tub packages containing of “BLOCK & BARREL IMPERIAL” White Meat Chicken Salad with a use-by date from May 22, 2017 through June 27, 2017.
  • 5-lb. plastic tub packages containing of “MARKET SOURCE” White Meat Chicken Salad with a use-by date from May 22, 2017 through June 27, 2017.
  • 5-lb. plastic tub packages containing of “DON’S SALADS” White Meat Chicken Salad with a use-by date from May 22 2017 through June 27, 2017.
  • 5-lb. plastic tub packages containing of “HYMIE’S” White Meat Chicken Salad with a use-by date from May 22, 2017 through June 20, 2017.
  • 5-lb. plastic tub packages containing of “DON’S SALADS” Chicken Waldorf Salad Made with White Meat Chicken with a use-by date from May 22, 2017 through June 20, 2017.
The products subject to recall bear establishment number “P-8429” inside the USDA mark of inspection. These items were shipped to distributors in Connecticut, Delaware, Maryland, Massachusetts, New Jersey, New York, Ohio, Virginia and Pennsylvania.
The problem was discovered on June 6, 2017, when Aldon Food Corporation received notification from one of their ingredient suppliers that the bread crumbs the company received and used in the recalled products potentially contained undeclared milk.
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 Deborah Rihs, General Manager, at (888) 321-3667. Media with questions about the recall can contact Mark Plamonden at (484) 533-3957.

New #foodsafety #recall #undeclared #milk #allergen in 4,335 lbs of ready-to-eat breaded chicken products

Water Lilies Food Inc., Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens

Class I Recall063-2017
Health Risk: HighJun 8, 2017
Congressional and Public Affairs
Jeremy J. Emmert
(202) 720-9113
Press@fsis.usda.gov
WASHINGTON, June 8, 2017 – Water Lilies Food Inc., a Astoria, N.Y., establishment, is recalling approximately 4,335 pounds of ready-to-eat breaded chicken products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products could contain milk, a known allergen, which is not declared on the product label. 
The Ahold Wedge spicy chicken tenders were produced on various dates from March 24, 27, and 28, 2017. The following products are subject to recall:
  • 10-oz. boxes of frozen “AHOLD WEDGE Spicy chicken strips fully cooked chicken breast tenders fritter with spicy seasoning.” 
The products subject to recall bear establishment number “P-21465A” inside the USDA mark of inspection. These items were shipped to retail locations in Connecticut, Delaware, District of Columbia, Massachusetts, Maryland, New Jersey, New York, Pennsylvania, Rhode Island and Virginia.
The problem was discovered on June 6, 2017, when the company received notification from an ingredient supplier that the bread crumbs the company received and used in the recalled products potentially contained undeclared milk.
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.  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 or media with questions about the recall can contact the company at (888) 387-7669.

New #foodsafety #recall #undeclared #milk #allergen in 174,000 lbs of various beef products

Maid-Rite Specialty Foods, LLC. Recalls Beef Products Due to Misbranding and Undeclared Allergens

Class I Recall061-2017
Health Risk: HighJun 8, 2017
Congressional and Public Affairs
Gabrielle N. Johnston
(202) 720-9113
Press@fsis.usda.gov
WASHINGTON, June 8, 2017 – Maid-Rite Specialty Foods, LLC., a Dunmore, Penn. establishment, is recalling approximately 174,000 pounds of various beef 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 products labels. 
The raw and ready-to-eat beef items were produced between March 13, 2017 and May 26, 2017. The following products are subject to recall: [View Labels (PDF only)]
  • 30-lb. bulk boxes of “FULLY COOKED BEEF BURGERS,” with case code 83353-52980 and lot numbers 04/04/17, 04/06/17, 04/07/17, 04/10/17, 04/18/17, 04/24/17, 04/25/17, 05/04/17, 05/08/17, 05/15/17 and 05/16/17.
  • 30-lb. bulk boxes of “FULLY COOKED BEEF BURGERS,” with case code 83353-52981 and lot numbers 03/31/17 and 05/08/17.
  • 30-lb. bulk boxes of “FULLY COOKED BEEF BURGERS,” with case code 83353-52982 and lot numbers 03/31/17, and 05/08/17.
  • 10-lb. bulk boxes of “FULLY COOKED AND CHARBROILED SALISBURY STEAK,” with case code 48339-44914 and lot numbers 03/31/17 and 05/08/17.
  • 10-lb. bulk boxes of “OUR HOMESTYLE BIG-N-BEEFY PATTIES,” with case code 70804-35001 and lot numbers 03/20/17 and 04/19/17.
  • 10-lb. bulk boxes of “OUR HOMESTYLE BIG-N-BEEFY PATTIES,” with case code 70804-35005 03/20/17, 03/31/17, 04/19/17, 05/02/17, 05/05/17, and 05/19/17.
  • 30-lb. bulk boxes of “FULLY COOKED BEEF MEATBALLS,” with case code 75156-33530with lot codes 03/13/17 and 04/28/17.
  • 10-lb. bulk boxes of “FULLY COOKED BEEF STEAKETTE FOR SALISBURY,” with case code 75156-34914 and lot number 04/27/17.  
  • 10-lb. bulk boxes of “FULLY COOKED AND CHARBROILED SALISBURY STEAK,” with case code 48339-44913 and lot numbers 03/16/17, 03/28/17, 04/18/17, 05/08/17, and 05/17/17.
The products subject to recall bear establishment number “EST. 77” or “EST. 118” inside the USDA mark of inspection. These items were shipped to institutional locations throughout the United States and Canada.
The problem was discovered on June 6, 2017, when Maid-Rite Specialty Foods, LLC. received notification from one of their ingredient supplier that the bread crumbs the company received and used in the recalled products potentially contained undeclared milk.
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 Kurt Sorensen or Deb Weber, Managers FSQA, at (570) 343-4748. Media with questions about the recall can contact Michael Bernstein, Vice President, at (570) 343-4748.

New #foodsafety #recall possible #Listeria #contamination of Happy Sprout Inc. Soybean Sprouts

Happy Sprout Inc. Recalls Soybean Sprouts Due To Possible Health Risk

June 8, 2017

Contact

Consumers

Happy Sprout Inc.
 703-832-1232
 804-786-3520

 

Announcement

Happy Sprout Inc. of Springfield, VA is voluntarily recalling all packages of soybean sprouts because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections to individuals 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 following products are being recalled by the firm.
  1. 1-lb bags of soybean sprouts in clear plastic bags labeled “GOODSEED Soy Bean Sprouts” “Keep Refrigerated” with a UPC Code of “21111 10035” produced on or after May 1, 2017.
  2. 2-lb bags of soybean sprouts in clear plastic bags labeled “GOODSEED Soy Bean Sprouts” “Keep Refrigerated” with a UPC Code of “21112 58772” produced on or after May 1, 2017.
  3. 10-lb bags of soybean sprouts in black plastic bags labeled with a sticker “GOODSEED Soy Bean Sprouts” produced on or after May 1, 2017.
These items were distributed to retail stores in Virginia, Maryland and New Jersey.
The potential for contamination was noted after routine surveillance sampling by the Virginia Department of Agriculture’s Food Safety Program and subsequent testing by the Virginia Division of Consolidated Laboratory Services revealed the presence of Listeria monocytogenes in sampled product. No illnesses have been reported to date.
Individuals who purchased GOODSEED brand soy bean sprouts distributed by Happy Sprout Inc. should return the product to the place of sale for a full refund.
Consumers with questions may contact the company directly at 703-832-1232 or the Virginia Department of Agriculture and Consumer Services, Food Safety Program at 804-786-3520.
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New #foodsafety #recall possible #glass #contamination in Southern Grove Cashew Halves and Pieces with Sea Salt

Star Snacks Co. is voluntarily recalling two lots of Southern Grove Cashew Halves and Pieces with Sea Salt due to the potential presence of glass pieces

June 6, 2017

Contact

Consumers

  RecallFEQ01@gmail.com
 201-882-4593

Media

Eddie Engelman
  RecallFEQ01@gmail.com
 201-882-4593

Announcement

Star Snacks Co. of Jersey City, NJ is voluntarily recalling  two lots of Southern Grove Cashew Halves and Pieces with Sea Salt due to the potential presence of glass pieces.
The affected product was distributed in 8.0oz canisters under the following label:
Southern Grove Cashew Halves and Pieces with Sea Salt, Net Weight 8.0 oz. (227 grams) 
UPC code 041498179366  
Code: Best by date 11/27/18 & 11/28/18 (printed on the bottom of the can)
No other product is affected by this voluntary recall.
The recall was initiated after the company received consumer reports of glass found in the product. To date, there have not been any reported injuries. Potentially impacted product has been removed from store shelves.
 
The product was distributed to ALDI stores in the following states: Alabama, Arkansas, California, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington DC., Wisconsin and West Virginia.
Consumers who have purchased the product in question are urged not to consume this product and may return the product to their local ALDI store for a refund or dispose of the item. Consumers with questions may contact Star Snacks at 201-882-4593 or RecallFEQ01@gmail.com, Monday-Friday 9 am – 2 pm EST.
 
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Updated #foodsafety #recall FDA Investigates Findings of Hepatitis A Linked to Frozen Tuna

FDA Investigates Findings of Hepatitis A Linked to Frozen Tuna

On this page:
The U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC), are assisting state and local officials in assessing the risk of hepatitis A virus exposure from contaminated frozen tuna sourced from Sustainable Seafood Company, Vietnam, and Santa Cruz Seafood Inc., Philippines. If unvaccinated consumers have consumed the recalled product within the last two weeks, post-exposure prophylaxis may help prevent hepatitis A virus infection.


Update

Prior to FDA’s announcement, Hilo Fish Company alerted its customers and distribution partners directly to let them know about the company’s voluntary recall of certain tuna products on May 18. The FDA received records from the company or its distribution partners indicating that they sold frozen tuna to the establishments listed on the FDA’s website. The FDA is working with Hilo and other distributors to ensure that the companies remove product from the market. The table containing the names of establishments have been updated.
It is the responsibility of the Hilo Fish Company to notify its customers about the voluntary recall. It is also the responsibility of any company that received a recall notice from Hilo Fish Company to notify its customers. The establishments identified on the FDA’s website should have received a notice from Hilo Fish Company or their direct supplier. If they have not, they should reach out to their suppliers for more information. Any company that has questions about the voluntary recall or has affected product and did not receive notice should contact the FDA at 1-800-SAFEFOOD.

Fast Facts

  • On May 18, Hilo Fish Company began recalling tuna sourced from Sustainable Seafood Company and Santa Cruz Seafood, Inc. that tested positive for the hepatitis A virus.
  • While the CDC is not currently aware of any illnesses linked to these products, it is advising post exposure prophylaxis (PEP) for unvaccinated persons who may have consumed the potentially contaminated tuna within the past two weeks. 
  • The FDA is providing a list of establishments in TX, OK, and CA that may currently have potentially contaminated tuna in commerce to help alert consumers that may be at risk of the hepatitis A virus. Contact your health care professional if you believe you have been exposed to contaminated tuna.
  • The current recall resulted from follow-up after the Hawaii Department of Health notified the FDA of a frozen tuna sample, sourced from PT Deho Canning Co.,which tested positive for hepatitis A on May 1, 2017. The initially recalled product has been removed from circulation and the newly recalled frozen tuna lots were not shipped to Hawaii, but were shipped to the mainland U.S.

What was the Problem and What was Done About It?

Consumers may be at risk of contracting a hepatitis A infection due to the consumption of potentially contaminated frozen tuna distributed by Hilo Fish Company and sourced from Sustainable Seafood Company (Lots F5-6 Soui Dau Industrial Zone, Can Lam Khanh Hoa Province, Vietnam) and Santa Cruz Seafood, Inc. (General Santos Fishport Complex Tambler, General Santos City, 9500, Philippines). The CDC reports no illnesses to date.
The FDA is collecting additional frozen tuna samples and increasing its screening measures and testing for imported seafood for these companies.
In addition, the agency has prepared a list of restaurants and other retail locations that received the recalled frozen tuna. The agency will continue to update this list as its investigation continues. To protect the health of consumers who may have eaten contaminated tuna and require post-exposure prophylaxis, the FDA has determined that it is necessary to make public the names of these businesses as part of the recall.

Background

On May 1, the Hawaii Department of Health notified the FDA that a sample of frozen tuna cubes from Indonesia tested positive for the hepatitis A virus. On May 2, the FDA contacted the Tropic Fish Hawaii LLC, a subsidiary distributor of Hilo Fish Company, to obtain additional information related to the positive tuna sample. Tropic Fish Hawaii LLC initiated a product recall because the affected product had been distributed to its customers in Oahu, Hawaii (U.S. mainland and other Hawaiian Islands were not affected by the recall). The state of Hawaii embargoed the lot that tested positive and the FDA confirmed the sample was positive.
On May 16, Hilo Fish Company notified the FDA that it had submitted samples of additional shipments held in its cold storage facility in Hawaii to a private laboratory for testing and received additional positive results for the hepatitis A virus. Imported tuna products from this facility were sourced from Sustainable Seafood Company and Santa Cruz Seafood and were distributed to restaurants and other retail locations in CA, NY, OK, and TX. The New York State Department of Health and the FDA verified that product shipped to New York was not sold to the public. The FDA’s investigation in connection with these firms is ongoing.

What is Hepatitis A?

Hepatitis A is a contagious liver disease that results from infection with the hepatitis A virus . It can range in severity from a mild illness lasting a few weeks to a severe illness lasting several months. Hepatitis A can be spread when a person ingests the virus from contaminated food or water. The virus can also be easily passed from an infected person to other unvaccinated family members, sexual partners, and close contacts.

What are the Symptoms of Hepatitis A?

Symptoms in adults include fatigue, abdominal pain, jaundice, abnormal liver tests, dark urine, and pale stool. People with hepatitis A may not have symptoms until 15 to 50 days after consuming a contaminated food or drink. CDC reports that while the hepatitis A vaccine is recommended for all children, vaccination rates are lower than for other recommended childhood vaccines. Unvaccinated children can become ill and not have symptoms.

Who is at Risk?

Any unvaccinated person who consumed recalled frozen tuna is at risk of contracting the hepatitis A virus.

What Can be Done to Prevent Infection with Hepatitis A?

CDC recommends providing post exposure prophylaxis (PEP) for unvaccinated people who have eaten any of the recalled raw or undercooked tuna products in the last two weeks. People who have consumed this fish fully cooked are at reduced risk of exposure, but we encourage consultation with medical professionals.
PEP consists of:
  • Hepatitis A vaccine for people between the ages of 1 and 40 years
  • Hepatitis A virus-specific immunoglobulin (IG) for people outside of this age range, but the hepatitis A vaccine can be substituted if IG is not available.
  • Those with evidence of previous vaccination do not require PEP
If you are unsure if you have been vaccinated against hepatitis A virus, contact your health professional to check your immunization records. If you have been vaccinated, no further action is needed. If you have never received the hepatitis A vaccine, getting a single dose within two weeks of exposure can protect against illness. If you are unable to determine whether you have already been vaccinated, receiving an additional dose of vaccine is not harmful.

What Specific Products Were Recalled?

The first recall, which took place in Hawaii, consisted of imported raw frozen ahi tuna cubes sourced from PT Deho Canning Co. (JL. Raya Madidir, Bitung, Indonesia). That recall by Tropic Fish includes lot codes 609149 and 609187. No products are believed to remain on the market.
The current recall, which began May 18, consists of frozen yellowfin tuna steaks from Sustainable Seafood Company and yellowfin tuna cubes from Santa Cruz Seafood. This recall by Hilo Fish Company includes Tuna Steaks, 8 oz. individually vacuum packed bags, production date code: 627152, Lot number: 166623; Expiration date: 2018-10-01 and Frozen Yellowfin tuna cubes, random; Individually vacuum packed; 15 lb. case, date code: 705342, Lot number: 173448; Expiration dates: 2019-04-01).
Name Location
Almansor Court 701 S. Almansor St., Alhambra, CA
Arroyo Trabuco 26772 Avery Pkwy, Mission Viejo, CA
Blue HI Café 2 Embarcardero, San Francisco, CA
Camp Four Wine Café 1508 10th St. Modesto, CA
Doubletree 555 W. Foothill Blvd., Claremont, CA
Fuzio’s 1020 10th St. Modesto, CA
High Sierra Grill House 2003 W. Bullard, Fresno, CA
Hotel Irvine 17900 Jamboree Rd, Irvine, CA
Jus Poke 501 N. Pacific Coast Hwy, Redondo Beach, CA
Noelani 1037 Laurel St. San Carlos, CA
Ola Mexican Kitchen Huntington Beach, CA 
Poke Shack 2001 Lawton St. San Francisco, CA
Shamrock Foods 12400 Riverside Dr. Eastvale, CA 

What Do Restaurants and Retailers Need To Do?

Prior to FDA’s announcement, Hilo Fish Company alerted its customers and distribution partners directly to let them know about the company’s voluntary recall of certain tuna products on May 18. The FDA received records from the company or its distribution partners indicating that they sold frozen tuna to the establishments listed on the FDA’s website. The FDA is working with Hilo and other distributors to ensure that the companies remove product from the market.

It is the responsibility of the Hilo Fish Company to notify its customers about the voluntary recall. It is also the responsibility of any company that received a recall notice from Hilo Fish Company to notify its customers. The establishments identified on the FDA’s website should have received a notice from Hilo Fish Company or their direct supplier. If they have not, they should reach out to their suppliers for more information. Any company that has questions about the voluntary recall or has affected product and did not receive notice should contact the FDA at 1-800-SAFEFOOD.

Affected restaurants and other retail locations should take appropriate actions to ensure that recalled product is not served to consumers. If any businesses find they served any recalled product within the last two weeks, they should contact their local health department and wherever possible, notify their consumers about possible exposure to hepatitis A virus and the potential benefit of post exposure prophylaxis.
In the event that retailers and/or other retail locations are found to have handled recalled or other potentially contaminated food in their facilities, they should:
  • Wash and sanitize display cases and refrigerators where potentially contaminated products were stored.
  • Wash and sanitize cutting boards, surfaces, and utensils used to prepare, serve, or store potentially contaminated products.
  • Wash hands with hot water and soap following the cleaning and sanitation process.
  • Retailers, restaurants, and other food service operators who have processed and packaged any potentially contaminated products need to be concerned about cross contamination of cutting surfaces and utensils through contact with the potentially contaminated products.

What Do Consumers Need To Do?

If you think you’ve gotten sick from eating recalled tuna contact your health care professional. The FDA and CDC are not currently aware of any illnesses related to any recalled frozen tuna. However, because hepatitis A can have serious health consequences, CDC advises post exposure prophylaxis (PEP) for unvaccinated persons who have consumed any of the recalled frozen tuna products in the past two weeks. PEP offers no preventive benefit to persons whose exposure occurred more than 2 weeks ago. People who have consumed this fish fully cooked are at reduced risk of exposure, but are encouraged to consult with their medical professionals.
Contaminated shellfish, fruit (berries), and salads are the most frequent foodborne sources of hepatitis A. Hepatitis A can be transmitted from person to person. Consumers should always practice safe food handling and preparation measures. Wash hands, utensils, and surfaces with hot, soapy water before and after handling food. Consumers should thoroughly wash their hands after using the bathroom and changing diapers to help protect themselves from hepatitis A, as well as other foodborne diseases.

Who Should be Contacted?

Contact your healthcare professional if you think you may have become ill from eating tuna, or if you believe that you have eaten any of the recalled frozen tuna within the last two weeks.

New #foodsafety #recall possible #Ecoli #contaminatino of 22,832 lbs of raw ground beef and beef primal cut products

Creation Gardens Inc. Recalls Ground Beef and Beef Primal Cut Products Due to Possible E. coli O157:H7 Contamination

Class I Recall059-2017
Health Risk: HighJun 5, 2017
Congressional and Public Affairs
Jeremy J. Emmert
(202) 720-9113
Press@fsis.usda.gov
WASHINGTON, June 5, 2017 – Creation Gardens, Inc., a Louisville, Ky., establishment, is recalling approximately 22,832 pounds of raw ground beef and beef primal cut products that may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw ground beef and beef primal cut products items were produced on May 31, June 1 and June 2, 2017. The following products are subject to recall: [View Labels (PDF only)]
  • 2, 20-lb. packages of “BEEF-GROUND COARSE 80/20” with product code 00297.
  • 48, 4-oz. packages of “BEEF-PATTIES ANGUS 4-1” with product code 00263.  
  • 48, 4-oz. packages of “BEEF-PATTIES ANGUS 4-1” with product code 11062.
  • 24, 10-oz. packages of “BEEF-PATTIES BLACK HAWK” with product code 97675.
  • 1, 60-lb. package of “BEEF-GROUND 80/20 W/SALT CK” with product code 00239.
  • 62, 60-lb. cases of “BEEF-GROUND BULK 80/20 W/SALT” with product code 00291.
  • 30, 6-oz. packages of “BEEF-PATTIES BLACK HAWK” with product code 97673.  
  • 30, 6-oz. packages of “BEEF-PATTIES STRIP-SHORT RIB” with product code 32100.
  • 1, 30-lb. packages of “BEEF-RIBEYE EXPORT BLACK HAWK” with product code 79684.
  • 24, 8-oz. packages of “BEEF-PATTIES BRISK-SHORT RIB” with product code 00274.
  • 30, 6-oz. packages of “BEEF-SIRLOIN C/C BLACK HAWK” with product code 00496.
  • 1 Case of “BFRESH-BEEF SLIDER 15-2 0Z” with product code 02374.
  • 30, 6-oz. packages of “BEEF, PATTIES 75/25 6 0Z STK PAC” with product code 00249.
  • 24, 10-oz. packages of “BEEF, PATTIES 75/25 10 0Z STK PA” with product code 00248.
  • 1, 10-lb. package of “BEEF-GROUND 80/20 HOUSE BRAND” with product code 00300.
  • 24, 7-oz. packages of “BEEF-PATTIES 100% NATURAL ANGU” with product code 00286.
  • 8, 8-oz. packages of “BFRESH-PATTIES BRISK/ SHORT RIB” with product code 02309.
  • 24, 7-oz. packages of “BEEF-PATTIES BLACK HAWK” with product code 77749.
  • 30, 6-oz. packages of “BEEF-SIRLOIN C/C BLACK HAWK” with product code 00496.
  • 24, 10-oz. packages of “BEEF-PATTIES BRISK-SHORT RIB” with product code 99943.
  • 1, 15-lb. package of “BEEF-RIBEYE LIPON BLACK HAWK” with product code 05471.
  • 24, 8-oz. packages of “BEEF-PATTIES ANGUS 2-1” with product code 00258.
  • 30, 5.3-oz. packages of “BEEF-PATTIES ANGUS 3-1” with product code 00261.
  • 1, 10-lb. package of “GROUND, BEEF 75/25 10#;” with product code 00232.
  • 1, 30-lb. package of “BEEF-RIBEYE EXPORT BLACK HAWK;” product code 79684.
  • 24, 8-oz. packages of “BEEF, PATTIES 75/25 2-1 STK PAC;” product code 00240.
  • 4, 10-lbs. packages of “BEEF-GROUND 80/20 HOUSE BRAND;” product code 00299.
The products subject to recall bear establishment number “EST. 7914” inside the USDA mark of inspection. These items were shipped to food service locations in Indiana, Kentucky, Ohio and Tennessee.
The problem was discovered on June 5, 2017 when plant management notified FSIS in-plant inspection personnel of two positives for E. coli O157:H7 test results.
E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2–8 days (3–4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160° F. The only way to confirm that the meat is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, http://1.usa.gov/1cDxcDQ.
Media and consumers with questions regarding the recall can contact Rob Webber, at (1-800-600-8510).

New #foodsafety #recall #undeclared #pecan & #treenut #allergen in Bakehouse Bread Cranberry Orange Bread

Fry’s Food Stores Issues Allergy Alert on Undeclared Pecans and Tree Nuts in Bakehouse Bread Cranberry Orange Bread

June 3, 2017

Contact

Consumers

Kroger
 1-800-KROGERS

Media

Pam Giannonatti
 (623) 907-4980

Announcement

Tolleson, AZ June 3, 2017 – Fry’s Food Stores has recalled Bakehouse Bread Cranberry Orange Bread sold in its retail stores because it contains undeclared pecans and tree nuts.  People who have an allergy or severe sensitivity to pecans or tree nuts run the risk of a serious or life-threatening allergic reaction if they consume these products.  Although pecans are listed in the ingredient statement, pecans or tree nuts are not included in the “Contains” statement.
People who have an allergy or severe sensitivity to pecans or tree nuts run the risk of a serious or life-threatening allergic reaction if they consume these products.  For consumers who are not sensitive to pecans or tree nuts, there is no safety issue with the product.  This recall was initiated because Fry’s was notified of this issue by a customer who consumed this product. One customer allergic reaction has been reported at this time. 
Product Description  UPC  Code  Size 
Bakehouse Bread Cranberry Orange Bread 864934 00004 lbs Sell By: June 07 2017 and Before  16 oz 
 
This recall includes all Fry’s Food Stores operating across Arizona.
Customers who have purchased any of the products described above and have sensitivity to pecans or tree nuts, 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.
Fry’s Food Stores is headquartered in Tolleson, Arizona. The company employs more than 20,000 Arizona residents. Fry’s has been serving Arizonans’ with fresh food at famous low prices since 1960. For more information about Fry’s Food Stores, visit the company’s website at www.Frysfood.com. Fry’s is a division of the Kroger Co.
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New #foodsafety #recall possible #Listeria #contamination of Global Garlic Inc. “Queso Freso/Whole Milk Cheese”

Global Garlic Inc. Recalls “Queso Freso/Whole Milk Cheese” Because of Possible Health Risk

June 7, 2017

Contact

Consumers

 (305) 545-6305

Announcement

Global Garlic Inc., 11501 NW 107th ST, Miami, FL, is recalling its 16oz packages of “Queso Fresco/ Whole Milk” and (“Queso Fresco x LB(Barra)/Whole Milk Cheese” because they have the potential to be contaminated with Listeria monocytogenes, and 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 stillbirth among pregnant women.
The recalled “Queso Fresco 16oz / Whole Milk” and (“Queso Fresco x LB (Barra)/Whole Milk Cheese” were distributed in Florida, Illinois, Kentucky, Louisiana and North Carolina.
The 16oz cheese comes in a clear plastic package marked with a UPC No. 8-96211-00235-9 and an expiration date of September 19, 2017 stamped on the side. The pound (barra) cheese weighted around 5-6 Lb., with a clear plastic package, it has no UPC number and expiration date of June 17, 2017.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after routine testing by the Florida Department of Agriculture Consumer Services revealed the presence of Listeria monocytogenes in 16 ounce packages of “Queso Fresco/ Whole Milk Cheese”.
The production of the product has been suspended while FDA and the company continue to investigate the source of the problem.
Consumers who have purchased 16oz packages of “Queso Fresco/ Whole Milk” and (“Queso Fresco x LB (Barra)/Whole Milk Cheese” are urged to return them to the place of purchase for full refund.
Consumers with questions may contact the company from Monday – Friday 8:00AM-5:30PM EST (305) 545-6305.
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New #foodsafety #recall possible #Alkaline Phosphatase in Half & Half in plastic gallon and pint bottles from Naturally Wholesome Products LLC

Naturally Wholesome Products LLC Wholesome Country Creamery LLC Voluntary recall of Half & Half in plastic gallon and pint bottles, due to the presence of Alkaline Phosphatase in samples

May 24, 2017

Contact

Consumers

 (336) 468-1520

Media

Rhoda Hostetler or Ruth Hostetler
 (336) 468-1520

Announcement

Naturally Wholesome Products LLC is voluntarily recalling gallon and pint containers of Half & Half labeled under the brand name Wholesome Country Creamery due to the presence of Alkaline Phosphatase found in samples during routine testing. Naturally Wholesome Products LLC has received no reports of illnesses related to the affected product and is removing the product from the market out of the abundance of caution.
All gallon and pint containers involved in this recall have a batch code of 4052917 or 2060517. Distribution of the affected product was limited in scope. No other Naturally Wholesome Products LLC products are affected by this recall.
The company initiated this voluntary recall because, in routine testing, samples of the affected product were found to contain Alkaline Phosphatase, an enzyme naturally present in raw milk but not in milk that has been properly pasteurized. The North Carolina Department of Agriculture and Consumer Services, during a follow-up investigation of the plant, identified 2 batches of Half & Half that were not pasteurized per the requirements of the Pasteurized Milk Ordinance.
The recall involves 244 units of the affected product which was distributed only in North Carolina. The company is actively notifying customers and is in the process of retrieving the affected product.
How to Identify The Recalled Product
This recall includes only gallon and pint containers of Half & Half that carry the Wholesome Country Creamery brand name. The containers have a small white sticker reading: 4052917 or 2060517.
No other Naturally Wholesome Products LLC products are included in this recall.
Naturally Wholesome Products LLC has ceased distribution of the affected product and recovery is actively underway. Consumers who have this product should not consume it. They should discard it and may return the product container to the place of purchase for a full refund or exchange. Consumers with questions can contact the company at (336) 468-1520.
Because the presence of Alkaline Phosphatase in milk suggests the milk may not have been pasteurized sufficiently, it is possible that pathogens present in the raw milk to begin with, including Salmonella, Campylobacter, Listeria, and/or E. coli, have survived and, if ingested, could cause gastrointestinal infection and its potential ensuing complications.
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