Based on information received from Kerry Ingredients & Flavours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary ST Specialty Foods, Inc. The recalled products include a seasoning blend manufactured by Kerry Ingredients & Flavours.
Category Archives: Food & Drug Recalls
U.S. Marshals seized misbranded drugs in Maine
On May 31, 2012, at the request of the U.S. Food and Drug Administration, U.S. Marshals seized drug products from Global Biotechnologies, Inc., of Portland, Maine, pursuant to a warrant issued by the U.S. District Court for the District of Maine.
Botanical Laboratories Inc. Recalls Wellesse Digestive 3 in 1 Health® Because of Possible Health Risk
Botanical Laboratories of Ferndale, WA is recalling 38 bottles of 33.8 oz “Digestive 3 in 1 Health ” liquid dietary supplement and 275 bottles of 16 oz. “Digestive Health 3 in 1” liquid dietary supplement, because a supplier of one of the ingredients has indicated the ingredient 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.
Sandoz US Announces Precautionary Recall Of Oral Contraceptive Introvale®, Following Report Of Packaging Flaw
Sandoz is conducting a voluntary recall of 10 lots of its generic oral contraceptive Introvale® in the US, following a recent report of a packaging flaw. The probability of this packaging flaw causing serious adverse health consequences is remote and Sandoz is not aware of any reports of related adverse events.
FDA issues alert on Reumofan Plus
Health officials in Mexico order recall based on potentially harmful pharmaceutical ingredients in Reuofan Plus. The U.S. Food and Drug Administration is warning consumers that Reumofan Plus, marketed as a “natural� dietary supplement for pain relief and other serious conditions, contains several active pharmaceutical ingredients not listed on the label that could be harmful.
An Updated Message to our Customers – Recall of South Korea Shellfish
On Friday, May 25, 2012, at the end of the business day, the FDA issued a Constituent Update on shellfish from Korea. This update supplemented an announcement released on May 18th, clarifying that canned product (now in addition to fresh and frozen shellfish from Korea) was considered adulterated.
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FDA warns consumers about counterfeit version of Teva’s Adderall
The U.S. Food and Drug Administration is warning consumers and health care professionals about a counterfeit version of Teva Pharmaceutical Industries’ Adderall 30 milligram tablets that is being purchased on the Internet. Adderall, which is approved to treat attention deficit hyperactivity disorders (ADHD) and narcolepsy, is a prescription drug classified as a controlled substance, a class of drugs for which special controls are required for dispensing by pharmacists.
OSKRI CORP. ISSUES ALLERGY ALERT on UNDECLARED CASHEWS in “PEACH GRANOLA”
OSKRI Corp. of Lake Mills, WI is recalling 3.53 ounce bags of “Peach Granola”, because it may contain undeclared cashews. People who have an allergy or severe sensitivity to cashews and/or other nuts run the risk of serious or life-threatening allergic reaction if they consume these products.
FDA warns consumers about counterfeit version of Teva’s Adderall
The U.S. Food and Drug Administration is warning consumers and health care professionals about a counterfeit version of Teva Pharmaceutical Industries’ Adderall 30 milligram tablets that is being purchased on the Internet. Adderall, which is approved to treat attention deficit hyperactivity disorders (ADHD) and narcolepsy, is a prescription drug classified as a controlled substance – a class of drugs for which special controls are required for dispensing by pharmacists.
The Menz Club, LLC . Issues a voluntary nationwide recall of V-Maxx Rx due to undeclared sulfoaildenafil
An FDA lab analysis of V Maxx Rx Lot # 101109 distributed by The Menz Club, LLC
was found to contain undeclared sulfoaidenafil. Sulfoaidenafil is an analog of sildenafil,
an FDA approved prescription drug used to treat Erectile Dysfunction (ED), making V
Maxx Rx, an unapproved new drug.