Tag Archives: Salmonella

U.S. Food & Drug Administration (FDA)


FDA (trade union)
FDA (trade union) (Photo credit: Wikipedia)
05/29/2013 03:06 PM EDT
FRUIT TREASURE of CHULA VISTA, CA is recalling 43 boxes (25lb) of fresh THAI PEPPERS, because it 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 often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
05/29/2013 06:17 PM EDT
Lowlite Investments d/b/a Olympia Pharmacy (“Lowlite”) today announced a voluntary multi-state recall of all sterile drug products compounded by the pharmacy that have not reached the expiration date listed on the product. The recall is being initiated due to concerns associated with prior quality control procedures that impacted sterility assurance.
05/29/2013 06:54 PM EDT
Today, Lightlife Foods in cooperation with the U.S. Food and Drug Administration (FDA) is voluntarily recalling a limited number of packages of its Lightlife Farmer’s Market Veggie Burgers that may contain an undeclared allergen, milk. Certain packages of the Farmer’s Market Veggie Burgers may have inadvertently been filled with Lightlife Kick Black Bean Burgers, which contain an allergen, milk. The milk allergen is not declared on the Farmer’s Market Veggie Burger product label. This product was shipped to food stores and distributors nationwide.

U.S. Food & Drug Administration (FDA)


Fda
Fda (Photo credit: Wikipedia)
05/02/2013 02:09 PM EDT
May 1, 2013 – American Lifestyle is announcing that it is conducting a voluntary recall of all lots of Vicerex UPC 893490820087 and Black Ant UPC 4026666142546. Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains undeclared sildenafil.
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04/30/2013 08:18 PM EDT
CARSON’S DELI & BAKERY of Lockport, NY is recalling 200 packages of ASSORTED COOKIE PACK, UPC 7 53182 15240 0, and FUDGE BROWNIE COOKIES, UPC 7 53182 15240 0 because they contain undeclared allergens. Carson’s Assorted Cookie Pack contains undeclared walnuts, wheat flour, milk and peanut butter.
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04/30/2013 08:16 PM EDT
Prime Food USA, 50st & 1st Ave Building # 57, Brooklyn NY 11232, is recalling Latis Brand Herring Fillet “Antalja” in Oil and Latis Brand Herring Fillet in Oil with Spices due to contamination with listeria monocytogenes. Listeria can cause serious complications for pregnant women, such as stillbirth.
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04/30/2013 12:27 PM EDT
Krinos Foods, LLC. of Long Island City, New York is voluntarily recalling its TAHINI sesame paste, because it 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 often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
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U.S. Food & Drug Administration (FDA)


English: Logo of the .
English: Logo of the . (Photo credit: Wikipedia)
04/23/2013 10:44 AM EDT
Nora Apothecary & Alternative Therapies today announced a voluntary multi-state recall of all sterile drug products compounded by the pharmacy that have not reached the expiration date listed on the product. The compounded products that are subject to the recall are those products within their expiration date that were compounded and dispensed by the pharmacy on or before Friday, April 19, 2013.
 
04/23/2013 10:47 AM EDT
On January 8, 2013, GE Healthcare initiated a nationwide voluntary field corrective action of the Giraffe Incubator with a Servo Control Oxygen System and Giraffe OmniBed, which were manufactured from August 1, 2012 through December 20, 2012. Giraffe Incubators without a Servo Control Oxygen System are not impacted.

Natura Pet Expands Voluntary Recall of Dry Pet Foods Due to Possible Health Risk.

Natura Pet Products is voluntarily expanding its March 29, 2013 recall of dry pet foods because they have the potential to be contaminated with Salmonella

04/22/2013 04:04 PM EDT
April 22, 2013 – Go Max Go Foods LLC, announces that it has taken the precautionary measure of voluntarily withdrawing a limited quantity of vegan candy bar products. These products contain the following statement on the front label: “dairy-free”, which may lead to confusion for people who have allergies to milk products
 
 

U.S. Food & Drug Administration (FDA)


04/12/2013 01:34 PM EDT
April 12, 2013 – Wild Blue Yonder Foods of Lynn, MA is voluntarily recalling 834 cases of Chappaqua Crunch GF (Gluten Free) Simply Granola with Flax & Fruit because they contain undeclared almonds. People who have an allergy or severe sensitivity to almonds and other tree nuts run the risk of serious or life-threatening allergic reaction if they consume this product.
04/10/2013 09:41 PM EDT
Henderson, NV, Green Valley Drugs is voluntarily recalling All Lots of All Sterile products compounded, repackaged, and distributed by the pharmacy due to lack of sterility assurance and concerns associated with the quality control processes. A full list of the recalled products is attached to this press release and can be accessed at greenvalleymed.com.
04/10/2013 08:08 PM EDT
Affirm XL, Inc. is conducting a voluntary recall to the consumer level after FDA lab analysis testing found the product to contain an analogue of sildenafil. Sildenafil is an active ingredient used in an FDA-approved product for the treatment of male Erectile Dysfunction (ED).
04/10/2013 04:41 PM EDT
Stryker Corporation (NYSE:SYK)announced today that its orthopaedic division has received notice that the U.S. Food and Drug Administration (FDA) has reviewed the voluntary recall of its ShapeMatch Cutting Guides and that it will be classified as a Class I recall. ShapeMatch Cutting Guides are intended to be used as patient specific surgical instrumentation to assist in the positioning of total knee replacement components intraoperatively and in guiding the marking of bone before cutting.

U.S. Food & Drug Administration (FDA)


03/21/2013 03:58 PM EDT
Jones Natural Chews Co of Rockford, IL is recalling 245 boxes of Woofers (beef patties) because it has the potential to be contaminated with Salmonella. Salmonella can affect animals and there is risk to humans from handling contaminated pet products.