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The FDA has recalled thousands of bottles of the antidepressant duloxetine, sold under brand name Cymbalta, due to the presence of a possibly cancer-causing chemical.
The Food and Drug Administration (FDA) issued a Class II recall of more than 7,100 bottles of the antidepressant duloxetine due to the possible presence of a carcinogen. Duloxetine belongs to a ...
A slew of recent recalls and warnings has called into question the safety of products designed to treat and maintain eye health. On Friday, the Food and Drug Administration warned consumers not to ...
The Food and Drug Administration announced a Class II recall for more than 7,000 bottles of an antidepressant due to a chemical.. The recall was initiated earlier this month on Oct. 10. Duloxetine ...
The FDA has now set a Class II risk — the highest possible class — on a recall for taco, quesadilla, stir fry, and salad meal kits distributed to 30 states originally issued in October. FDA ...
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
The recall, initiated by Perrigo Company plc, involves 16,500 cans distributed to retailers across 12 states: The cans were sold at CVS stores in Florida, California, South Caroline, Virginia ...
The FDA has removed the following items from store shelves this September, including pet food, baby powder and Lactaid. Skip to main content. 24/7 Help. For premium support please call: 800-290 ...