The U.S. Food and Drug Administration announced today that USPlabs LLC, of Dallas, Texas, is recalling certain OxyElite Pro dietary supplement products that the company markets. The company took this action after receiving a letter from the FDA stating that the products have been linked to liver illnesses and that there is a reasonable probability that the products are adulterated.
Atherstone Foods Voluntarily Recalls Salads and Wraps Because of Possible Health Risk
Athertone Foods, Inc. of Richmond, CA is voluntary recalling “Best Buy” dates 9-23-13 through 11-14-13 of ready to eat salads and wraps 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.
USPlabs LLC Announces a Recall of OxyElite Pro Dietary Supplements Due to Possible Health Risk
USPlabs LLC, Dallas, TX is voluntarily conducting a national recall of all
lots and sizes of the OxyElite Pro dietary supplement products listed below.
These products contain Aegeline, a synthesized version of a natural extract from the Bael tree.
Read The Complete Story!
Plum Organics Voluntarily Recalls a Range of Pouch Products
Plum Organics is voluntarily recalling pouch products within its Baby Stage 2, Tots Mish Mash and Kids lines after discovering a manufacturing defect that may cause spoilage in some pouches. Recalled products can be identified by the “Best By” dates ranging from 08/05/14 to 12/08/14 and the letters “AT.”
Vega Issues Voluntary Withdrawal of Vega One Nutritional Shakes and Vega Sport Performance Protein Product Due to Traces of the Antibiotic Chloramphenicol
Sequel Naturals Inc., dba “Vega,” announced today that it has taken the precautionary measure of voluntarily withdrawing a limited quantity of its Vega One Nutritional Shakes and Sports Performance Protein products due to finding trace amounts of chloramphenicol (CAP), a naturally occurring antibiotic. Chloramphenicol is a prescription drug commonly used to treat typhoid fever and eye infections around the world. It should only be used under medical supervision.
FDA approves Aptiom to treat seizures in adults
The U.S. Food and Drug Administration today approved Aptiom (eslicarbazepine acetate) as an add-on medication to treat seizures associated with epilepsy.
FDA approves first generic versions of Aciphex delayed-release tablets to treat GERD
The U.S. Food and Drug Administration today approved the first generic versions of Aciphex (rabeprazole sodium) delayed-release tablets, used to treat gastroesophageal reflux disease (GERD) in adults and adolescents (ages 12 and up).
FDA takes action to speed safety information updates on generic drugs
A proposed U.S. Food and Drug Administration rule would speed the dissemination of new safety information about generic drugs to health professionals and patients by allowing generic drug makers to use the same process as brand drug manufacturers to update safety information in the product labeling.
Garden-Fresh Foods, Inc. Expands Recall Due to Potential Contamination with Listeria Monocytogenes
Garden-Fresh Foods has initiated an expansion of previous recalls of fresh cut vegetables, ready-to-eat salads, slaws, dips and spreads sold under various brands and code dates manufactured prior to November 06, 2013. All packaging types and sizes are included.
Read The Complete Story!
FDA takes step to further reduce trans fats in processed foods
The U.S. Food and Drug Administration announced its preliminary determination that partially hydrogenated oils (PHOs), the primary dietary source of artificial trans fat in processed foods, are not “generally recognized as safe” for use in food. The FDA’s preliminary determination is based on available scientific evidence and the findings of expert scientific panels.