BATTLE CREEK, Mich., Jan. 27, 2011 – Keebler® is recalling a limited quantity of 8-count cartons of Fudge Shoppe® Jumbo Fudge Sticks sold at convenience stores. This recall was initiated because the cartons contain individually wrapped Jumbo Peanut Butter Sticks. The individually wrapped cookie sticks are correctly labeled.
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Fourth FDA orphan drug designation workshop scheduled for Feb. 28 – March 1, 2011
The U.S. Food and Drug Administration has scheduled its fourth orphan drug designation workshop for academics, biotechnology companies, and those unfamiliar with the process for Feb. 28 – March 1, 2011, in Claremont, Calif. in collaboration with Keck Graduate Institute.
Important information for ARIXTRA® Starter Kit patients regarding Triad Group’s alcohol prep products
GlaxoSmithKline (GSK) has become aware of a United States market recall of all lots of alcohol prep pads, swabs and swabsticks manufactured by the Triad Group and marketed under various brand names. The Triad Group recall has been initiated due to concerns about potential microbial contamination of the alcohol products with Bacillus cereus that could potentially lead to life-threatening infections.
PEEKAY INTERNATIONAL INC. ISSUES ALLERGY ALERT ON UNDECLARED SULFITES IN SWAN GOLDEN RAISINS
PEEKAY INTERNATIONAL INC. is recalling SWAN GOLDEN RAISINS because they may contain undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume these products.
FDA review indicates possible association between breast implants and a rare cancer
ALCL, breast implants
State Garden, Inc. Announces Voluntary Recall Of Certain Salad Mixes Due To Possible Health Risk
State Garden, Chelsea, MA – is conducting a voluntary recall of all Salad products produced in our plant on January 4, 2011 which correspond to trace back codes 45693 and 45703 due to a risk of contamination with Listeria monocytogenes. Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
Pfizer Inc. And Progenics Alert Physicians And Patients To Information Related To Triad Group Alcohol Prep Products Included In U.S. RELISTOR Kit Packaging
NEW YORK, N.Y. and TARRYTOWN, N.Y. – Pfizer Inc. and Progenics
Pharmaceuticals, Inc. have learned of a United States market
recall of alcohol prep pads and swabs manufactured by the Triad
Group. In the interest of patient safety, Pfizer and Progenics
are alerting U.S. patients and physicians to Triad’s recall.
Ian’s Voluntarily Recalls Two Products Due To Risk Of Contamination By Listeria Bacteria
Ian’s is voluntarily recalling specific lot numbers of two products due to a risk of contamination with Listeria monocytogenes.
Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
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Kanec USA, Inc. Issues a Voluntary Recall of Nite Rider Maximum Sexual Enhancer For Men and STUD Capsules for Men Male Enhancement Herbal Supplement Capsules Marketed as Dietary Supplements
Kanec USA Inc., announced today that it is conducting a voluntary recall of All Lots of the company’s Nite Rider Maximum Sexual Enhancer For Men and STUD Capsule for Men because they were found adulterated with Sildenafil, an FDA approved drug used in the treatment of Erectile Dysfunction (ED), making the products unapproved new drugs. Representatives of the Food and Drug Administration (FDA) informed Kanec USA, Inc. of the laboratory analysis.
King & Prince Seafood Issues Voluntary Recall Notice On Breaded Calamari Products
King & Prince Seafood of Brunswick, Ga., is recalling its Breaded Calamari Rings. This recall is the result of notification by our supplier of these products that there may have been a potential peanut allergen cross-contamination during the manufacturing of soy flour, which is an ingredient in these products.
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