McAllen, TX Magic Valley Fresh Frozen, Inc. announced today that it is voluntarily recalling breaded okra produced under the HEB label from July 1, 2010 through January 31, 2011 because the product may contain undeclared whey (a milk ingredient).
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f’real® foods Issues Voluntary Recall of Strawberry Banana Smoothies Due to Potential Peanut Content
f’real® foods announced today a voluntary recall of f’real®Strawberry Banana Smoothies (Lot # 06/21/2012) produced at Smith Dairy Products Company in Orrville, Ohio. The company is recalling one specific lot as it may contain peanuts, an undeclared allergen.
St James Smokehouse, Inc, Announces Voluntary Recall of Scotch Reserve Whiskey & Honey Smoked Salmon 4oz Retail Packs Due To Possible Health Risk
St James Smokehouse Inc, is conducting a voluntary recall of Scotch Reserve Whiskey & Honey Smoked Scottish Salmon 4oz retails packs under Lot code:5797 & batch code: 4759 with UPC# 853729001151 due to potential contamination with Listeria Monocytogenes.
Neuro Resource Group, Inc. Informs Customers of Important Information about Triad Group’s Alcohol Prep Pads
Neuro Resource Group, Inc. (NRG) has become aware of the market recall of Triad Group’s alcohol prep pads, alcohol swabs, and alcohol swabsticks manufactured by Triad in the United States and marketed under various brand names. The Triad Group alcohol prep pads are co-packaged and distributed with NRG devices to customers in the United States and internationally.
FDA approves 1st pacemaker designed to work safely during some MRI exams
The U.S. Food and Drug Administration today approved the first heart pacemaker designed to be used safely during certain magnetic resonance imaging (MRI) exams.
BIOSAN LABORATORIES ISSUES ALLERGY ALERT ON UNDECLARED SOY IN VITAMIN AND NUTRITIONAL SUPPLEMENTS
BioSan Laboratories, Inc is conducting a voluntary recall on its products sold under the EssentialsTM and RightFoodTM Brands, as well as Therapeutix Cardio Strength and Innate Cardio Response. These products may contain undeclared soy flour.
FDA launches Medical Device Innovation Initiative
Today the U.S. Food and Drug Administration proposed the Innovation Pathway, a priority review program for new, breakthrough medical devices and announced the first submission: a brain-controlled, upper-extremity prosthetic that will serve as a pilot for the program. The FDA also announced plans to seek further public comment before the Pathway can be used more broadly.
FDA orders postmarket surveillance of certain TMJ implants
TMJ, postmarket, surveillance
Qualitest Pharmaceuticals Issues Voluntary, Nationwide Recall Of Hydrocodone Bitartrate And Acetaminophen Tablets, USP 10 MG / 500 MG, NDC 0603-3888-20, 60 Count, Lot Numbers T150G10B, T120J10E And T023M10A And Phenobarbital Tablets, USP 32.4 MG, NDC 0603-5166-32, 1000 Count, Lot Numbers T150G10B, T120J10E And T023M10A
Qualitest Pharmaceuticals today issued a voluntary nationwide recall of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10mg / 500mg, NDC 0603-3888-20, 60 count, Lot Numbers T150G10B, T120J10E and T023M10A, and Phenobarbital Tablets, USP 32.4 mg, NDC 0603-5166-32, 1000 count, Lot Numbers T150G10B, T120J10E and T023M10A. An individual bottle of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10mg / 500mg, NDC 0603-3888-20, 60 count was found incorrectly labeled with a Phenobarbital Tablets, USP 32.4 mg, NDC 0603-5166-32, 1000 count label, printed with Lot Number T150G10B. Lots T120J10E and T023M10A used the same stock inventory of labels as Lot T150G10B and are potentially impacted.
Rouses Markets Voluntarily Recalls Frozen Yellow Fin Tuna Steaks Due To Possible Health Risks
Rouses Markets (www.rouses.com) announced the voluntary recall of wild-caught yellow fin tuna steaks labeled as product of USA with a UPC Code beginning with 208732 sold at Rouses Markets with Sell By dates between December 1, 2010 and January 27, 2011. These previously frozen tuna steaks are being recalled because of potential elevated levels of histamine.