WellPet LLC announced a voluntary recall of one recipe of Wellness® dry dog food after being notified by Diamond Pet Foods regarding the presence of Salmonella in Diamond’s Gaston, South Carolina facility. All Wellness products are tested for Salmonella and all lots tested negative prior to shipping to customers.
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UPDATED: CORRECT PRODUCTION CODE INFORMATION Diamond Pet Foods Expands Voluntary Recall of Dry Pet Food Due to Potential Salmonella Contamination
Diamond Pet Foods today announced that it is expanding a voluntary recall to include batches of nine brands of dry pet food formulas manufactured between December 9, 2011 and April 7, 2012 due to potential Salmonella contamination. In April 2012, Diamond Pet Foods initiated three voluntary recalls of Diamond manufactured dry dog food.
Funfresh Foods, Inc. Voluntarily Recalls World Berries™ Organic “Cacao Nibs” Because of Possible Health Risk
FunFresh Foods, Inc. of San Clemente, California in consultation with the FDA is voluntarily recalling a single lot of its 6 ounce packages of FunFresh Foods™ World Berries™ Organic “Cacao Nibs” because they may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools.
FIGI’S INC. Issues Allergy Alert On Undeclared Almonds In Lemon Bar Bliss
Figi’s Inc, Marshfield, WI is recalling 51 units of the product Lemon Bar Bliss (1#tins), because it contains undeclared Almonds.
H-E-B Issues a Precautionary Recall For Asian Ready-to-Eat Meals due to Possible Health Risk
H-E-B has issued a voluntary and precautionary recall for certain Asian Ready-to-Eat meals due to the possibility of undercooked chicken in those meals. There have been no confirmed illnesses reported related to this precautionary recall.
Notice of Recall – Triamcinolone acetonide P.F. 80mg/ml
Franck’s lab recently had a fungal issue with one lot of triamcinolone acetonide P.F. 80mg/ml and on March 29, 2011 instituted a recall. The recall involved five physicians and eight prescriptions.
Church & Dwight Co., Inc. Voluntarily Recalls Select Lots of Spinbrush® Rechargeable SONIC Toothbrushes Distributed Between February 2010 and October 2011 for Possible Health Risk
Church & Dwight Co., Inc. is voluntarily recalling Spinbrush Rechargeable SONIC toothbrushes because the charging base may overheat with localized melting and sparking, possibly causing fire, shock or burns. The risk of these malfunctions appears to increase with the age of the product.
FDA issues final rule on sterility testing of biological products
The U.S. Food and Drug Administration issued its final rule on sterility testing, amending the requirements for most licensed biological products.
FDA permits marketing of a new device for abdominal surgery
On April 30, the U.S. Food and Drug Administration today allowed marketing of the first surgical instrument set that can be assembled and disassembled inside the body during surgery.
The Percutaneous Surgical Set is intended to be used during minimally invasive laparoscopic abdominal surgery, in which a camera and surgical instruments are inserted through one or more small incisions (surgical cuts into body tissue) in the abdomen.
FDA approves new orphan drug to treat a form of Gaucher disease
The U.S. Food and Drug Administration today approved Elelyso (taliglucerase alfa) for long-term enzyme replacement therapy to treat a form of Gaucher disease, a rare genetic disorder.