Thomas Produce Recalls Cucumbers because of Possible Health Risk

Consumers: Richard Wilson
 1-561-482-1111

Thomas Produce Company of Boca Raton, FL is recalling 174 bulk-packed containers of Cucumbers. This product has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella may experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain.

This product was sold to distributors in Florida and Georgia between 12/15/2015 and 12/16/2015. All distributors that received this product have been notified as of the time of this press release.

The fresh, whole, green Cucumbers were sold in 166 cardboard bushel boxes (1 1/9 bushel size) with one of the following lot numbers ink-jet printed on the side: 1554311JDNK, 1554311HDNK, and 15143115DNK. These cucumbers were also distributed in 8 bulk cardboard bins(4’x4′ size) tagged with codes 15NKJD-1554311-D, 15NKHD-1554311-D, and 15NK5D-1514311-D.

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

This recall notice is being issued due to an isolated instance in which a sample of Thomas Produce Cucumbers yielded a positive result for Salmonella in a random sample test conducted by the FDA. Out of an abundance of caution, the company has elected to recall all lots of cucumbers that were packed on the same day. The company has ceased production and distribution of the affected lots of cucumbers as the FDA and the company continue their investigation.

Consumers who have purchased these products are urged to not consume them. These products should be thrown away or returned to the original place of purchase. Consumers with questions may contact Richard Wilson, Compliance Director, of Thomas Produce Company at 1-561-482-1111 Monday through Friday between 9:00 a.m. and 4:30 p.m. EST.

Urgent: Drug Recall – Weight Loss Dietary Supplements with Undeclared Sibutramine and Phenolphthalein

Consumers: Toni Sweeney
 beextremellc@gmail.com
 814-771-4377

Under the brands: La’ Trim Plus, Jenesis and Oasis, all lots and expiration dates.

Recent Analysis by the Food and Drug Administration has found undeclared Sibutramine and Phenolphthalein in the Dietary Supplement “La’Trim Plus”, “Oasis”, and “Jenesis”. As a Seller of these products, my customer’s health is my first priority, therefore BeeXtreme LLC is recalling all lots of La’ Trim Plus, Jenesis and Oasis products from the market.

Sibutramine and Phenolphthalein pose a significant health hazard. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010. It is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. Phenolphthalein is an ingredient previously used in over-the-counter laxatives, but because of concerns of carcinogenicity, it is not currently approved for marketing in the United States. Health risks associated with phenolphthalein could include potentially serious, gastrointestinal disturbances, irregular heartbeat, and cancer with long-term use.

Please determine if you have any of the above products on hand. If so, please discontinue selling the products and do not consume them. Please promptly dispose of all identified products.

If you have further distributed La’ Trim, Jenesis and/or Oasis, please contact your customers if possible and advise them of the recall situation. Provide them with a copy of this notice. Have them return their outstanding recalled stocks to you. If you have any questions regarding this recall please contact me at beextremellc@gmail.com or 814-771-4377.

Ocean Group, Inc. Announces Recall of Ocean Brand Masago Lake Smelt Roe for Undeclared Allergens

Consumers: Kurt Kim: 213-272-2758

Los Angeles, CA-Ocean Group, Inc. of Los Angeles, CA is recalling Ocean brand Masago Lake Smelt Roe product because product labels failed to declare food allergens Wheat and/or Soy, in their ingredient statements. People who have an allergy or severe sensitivity to wheat or soy run the risk of a life threatening allergic reaction, anaphylaxis, that requires immediate medical attention should they consume this product. Recalled product is identified as follows:

Masago Lake Smelt Roe is a 6.0 oz. clear cup with the red marking “MASAGO” label on the top and the lid and the Nutrition Facts on the side of the cup.

Ocean Group, Inc. immediately segregated its entire inventory of recalled products and is notifying consumers and customers not to consume them. Ocean Group, Inc. wants to ensure its products are safe. Consequently, in addition to its ongoing cooperation with the California Department of Public Health, Ocean Group, Inc. is voluntarily recalling all aforementioned products from its customers. Consumers in possession of this product should not eat them, rather product should be returned to the place of purchase.

Ocean Group, Inc. will be sending recall notices to all of its direct customers . Please call Kurt Kim at (213) 272-2758 for further information.

Bellisio Foods, Inc. Recalls Boneless Pork Rib Frozen Entree Products Due To Possible Foreign Matter Adulteration

Class II Recall149-2015

Health Risk: Low

Dec 22, 2015

Congressional and Public Affairs
Kristen Booze
(202) 720-9113

WASHINGTON, Dec. 22, 2015 – Bellisio Foods, Inc., a Jackson, Ohio establishment, is recalling approximately 285,264 pounds of boneless pork rib shaped patty frozen entree products that may be adulterated with extraneous materials, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The Boston Market Boneless Pork Rib Shaped Patty with BBQ Sauce and Mashed Potatoes frozen entree items were produced on various dates between Sept. 09, 2015, and Dec. 14, 2015. The following products are subject to recall: [View Label (PDF Only)]

14-oz. boxed packages containing “Boston Market Home Style Meals Boneless Pork Rib Shaped Patty with BBQ Sauce and Mashed Potatoes” with Use By dates 09/09/2016; 09/22/2016; 10/08/2016; 10/30/2016; and 12/14/2016.

The products subject to recall bear establishment number “EST. 18297” on the end panel of the package. These items were shipped to retail locations nationwide.

The problem was discovered after the firm received consumer complaints of possible glass or hard plastic pieces being found in the frozen entree.

There have been no confirmed reports of adverse reactions or injuries 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 Consumer Relations at 1-855-871-9977. Media with questions about the recall can contact Tom Lindell, Public Relations, at (612) 305-6149.

The Cure House Recalls Pork Products Produced Without Benefit Of Inspection

Class I Recall148-2015

Health Risk: HighDec 19, 2015

Congressional and Public Affairs
Gabrielle N. Johnston
(202) 720-9113

WASHINGTON, Dec. 19, 2015 – The Cure House, a Louisville, Ky. establishment, is recalling an undetermined amount of cured pork products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The cured ham items were produced from 2009 thru Dec. 19, 2015. The following products are subject to recall:      

Various weights of individually wrapped “Woodland’s Pork Mountain Ham” products with no label.

The products subject to recall bear establishment number “Est. 44888” inside the USDA mark of inspection; however, this firm was not issued a USDA grant of inspection by FSIS. These items were shipped to distributors in Kentucky and New Jersey.                                

The problem was discovered when FSIS was alerted by the State of Kentucky, Food Safety Branch, of an operation receiving federally inspected not-ready-to-eat (NRTE) hams and further processing these hams without the benefit of FSIS inspection. A subsequent Office of Investigation, Enforcement, and Audit (OIEA) investigation confirmed the allegation on Dec. 17, 2015.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers and media with questions about the recall can contact Jay Denham, Operator, at (502) 235-3792.

Voluntary Recall Notice for Zatarain’s Red Beans and Rice Original due to Possible Health Risk from Undeclared Ingredients

Zatarain’s Consumer Affairs team
 1-877-837-3796
laurie_harrsen@mccormick.com
 (410) 527-8753

GRETNA, La. – Zatarain’s is initiating a voluntary recall of 8 oz boxes of Red Beans and Rice Original with a “BEST BY” date of  JUL 31 16Z distributed in the Midwest and Eastern regions of the U.S.  The Red Beans and Rice Original product may actually contain Creamy Parmesan Rice Mix with dairy ingredients.  Dairy allergens are not labeled on the Red Beans and Rice Original package.  People with a dairy allergy or sensitivity run the risk of a serious or life threatening allergic reaction if they consume this product.

No illnesses or allergic reactions have been reported to date and no other Zatarain’s products are involved in this recall.

The product subject to this recall is:

Zatarain’s Red Beans and Rice Original 8 oz box
PACKAGE UPC NUMBER: 7142909849
AFFECTED DATE CODE: BEST BY JUL 31 16Z
SHIPPING DATES: August 7, 2015 through September 29, 2015
STATES SHIPPED TO: FL, GA, IL, IN, KY, LA, MA, ME, MI, MN, MS, NC, NY, OH, PA, SC, TN, VA, and WI

All retail outlets that sell these products are being notified to remove the product with affected date code from their shelves and warehouses immediately.

Consumers do not need to return the product to the store where it was purchased.  Instead, consumers are urged to dispose of the product and do not consume the product.  Consumers may contact Zatarain’s Consumer Affairs team at 1-877-837-3796 weekdays from 9:30 AM to 7:00 PM (Eastern Time) for a replacement or full refund, as well as with general inquires.

This recall is being made with the knowledge of the Food and Drug Administration.  The Company is also issuing an alert through the Food Allergy & Anaphylaxis Network.

Stella & Chewy’s Voluntarily Recalls Frozen Dinner Morsel Products Due to Possible Health Risk

Customer Service
 info@stellaandchewys.com
 888.477.8977

Stella & Chewy’s is voluntarily recalling four of its products sold in the U.S. and Canada due to concerns of a possible presence of Listeria monocytogenes. The recall affects a total of 990 cases (964 cases in the U.S and 26 cases in Canada). The recall was prompted by a positive test confirming Listeria monocytogenes in Stella’s Super Beef Dinner Morsels for Dogs 8.5 oz. frozen bags, lot #165-15, “Use by 6-25-2016”, during routine surveillance testing by the Michigan Department of Agriculture and Rural Development.

Listeria is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.

As a precautionary measure, Stella & Chewy’s is voluntarily recalling all products from Lot # 165-15, which includes:

Product DescriptionSizeUPCLot #Use ByFrozen Stella’s Super Beef Dinner Morsels for Dogs8.5 oz.186011 001554165-156/25/2016Frozen Stella’s Super Beef Dinner Morsels for Dogs4 lb.186011 001370165-156/25/2016 & 6/26/2016Frozen Duck Duck Goose Dinner Morsels for Cats1.25 lb.186011 001455165-156/25/2016

Moreover, while the below listed product has not tested positive for Listeria monocytogenes, in an abundance of caution, we are also recalling the following products which may have come into contact with the affected lot:

Product DescriptionSizeUPCLot #Use ByFrozen Chick Chick Chicken Dinner Morsels for Cats1.25 lb.186011 001448160-157/2/2016Frozen Chick Chick Chicken Dinner Morsels for Cats1.25 lb.186011 001448152-157/2/2016

Retailers and consumers can find the full product recall list and additional information at: http://www.stellaandchewys.com/stella-chewys-recall-notice/.

Consumers should look at the product descriptions, UPCs, lot numbers, and “Use By” dates on each bag for an exact match to determine if it is subject to the recall. Anyone who has purchased these products are instructed to dispose of the food or return it to the place of purchase for a full refund.

Trader Joe’s Issues Voluntary Recall of Triple Ginger Brew

Customer Relations: (626) 599-3817

Trader Joe’s of Monrovia, CA is issuing a voluntary recall of all codes purchased from 11/9/15 through 12/14/15 of Triple Ginger Brew (SKU 51857) due to reports of unopened bottles potentially bursting. Although the ginger brew does not pose a health risk if consumed, all product has been removed from store shelves and destroyed. No injuries or illnesses have been reported to date.

This precautionary action comes after the company received inquiries from customers that had experienced unopened bottles shattering or bursting. The potentially affected product was distributed to Trader Joe’s stores nationwide. Trader Joe’s Triple Ginger Brew is sold in 25.4 FL OZ (750 mL) glass bottles.

Customers who have purchased the Trader Joe’s Triple Ginger Brew are encouraged to handle it with care and dispose of it immediately in an outside container. Trader Joe’s will provide a refund to customers who purchased the Triple Ginger Brew at any of their store locations. Customers can call the company’s Customer Relations at (626) 599-3817 6:00AM-6:00PM PST, Monday – Friday, with any questions.