Today, ConAgra Foods, in cooperation with the U.S. Food and Drug Administration (FDA), is recalling a limited number of Kroger’s Break ‘N Bake chocolate chip cookie dough packages due to peanut butter cup cookie dough inadvertently mispacked into chocolate chip cookie dough packages. 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.
Category Archives: Food & Drug Recalls
REACTION NUTRITION, LLC issues allergy alert on undeclared milk in LIVE CLINICAL 90 CAPS
Reaction Nutrition, LLC of Carnegie, PA is recalling LIVE CLINICAL 90 CAPS, because it contains undeclared milk. People who have an allergy or severe sensitivity to milk (bovine colostrum powder) run the risk of serious or life-threatening allergic reaction if they consume this product.
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New test system identifies 193 different yeasts and bacteria known to cause illness
The U.S. Food and Drug Administration today allowed marketing in the U.S. of the first mass spectrometer system for automated identification of bacteria and yeasts that are known to cause serious illness in humans. The VITEK MS can identify 193 different microorganisms and can perform up to 192 different tests in a single automated series of testing, with each test taking about one minute.
Jack Rabbit Inc. Conducts Voluntary Nationwide Recall of Lot 2510 of Jack Rabbit Dietary Supplement Due to undeclared ingredient
Jack Rabbit Inc. announced today that it is conducting a voluntary nationwide recall of one lot of the company’s dietary supplement product sold under the following name: Jack Rabbit. The product was found to contain Sildenafil and Tadalafil.
Terri Lynn, Inc. Issues Allergy Alert on Possible Undeclared Peanuts in its Packages of Deluxe Mixed Nuts
Terri Lynn, Inc. of Elgin, IL, is recalling 855 packages of its Deluxe Mixed Nuts because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Covidien Initiates a Voluntary Recall of Certain Lots of Monoject Prefill Flush Syringes Sold in the United States and Bermuda
August 19, 2013 – Mansfield, MA – Covidien today announced that it has initiated a voluntary recall of certain lots of Monoject prefill flush syringes. Reasons for Recall: This recall is being conducted due to the risk that a number of the syringes were filled with water but not subjected to the autoclave sterilization process.
See’s Candies, Inc. Issues Allergy Alert On Undeclared Milk In Dark Chocolate Blueberries
See’s Company of San Francisco is recalling all Dark Chocolate Blueberries because it contains undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.
Herbal Give Care LLC Issues Voluntary Nationwide Recall of Esbelder Man Capsules, Esbelder Fem Capsules, and Esbelder Siloutte Capsules Vitamin Supplements Due to Potential Health Risks
Grand Prairie, Texas, Herbal Give Care LLC is voluntarily recalling all lots of Esbelder man (30 capsules), Esbelder fem (30 capsules) and Esbelder siloutte (30 capsules) to the consumer level. The products have been found to contain undeclared Sibutramine, N-Desmethylsibutramine, and N-di-Desmethylsibutramine.
Buurma Farms, Inc. Recalls Fresh Cilantro Due to Possible Health Risk
Buurma Farms, Inc. is voluntarily recalling 465 boxes of Cilantro Lot #02D312A4. Buurma Farms recalled this product due to possible Listeria monocytogenes contamination, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
FDA reminds health care providers not to use sterile products from NuVision Pharmacy
The U.S. Food and Drug Administration is reminding health care providers about safety concerns with all sterile drug products made and distributed by NuVision Pharmacy of Dallas, Texas. Health care providers should not administer any NuVision Pharmacy sterile products to patients because the products’ sterility is not assured.