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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.
These items were compiled from the Food and Drug Administration's (FDA) list of "Recalls, Market Withdrawals & Safety Alerts." The list is not all-inclusive. The list is not all-inclusive.
Consumers and food establishments are urged to stop using these products immediately and follow the FDA's guidance on the recall. For more information, visit the FDA's official website. This ...
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]
The law grants the FDA a number of new powers, including mandatory recall authority, which the agency had sought for many years. The FSMA requires the FDA to undertake more than a dozen rulemakings and issue at least 10 guidance documents, as well as a host of reports, plans, strategies, standards, notices, and other tasks.
It’s also important to constantly check the FDA and USDA's FSIS recall pages to stay up to date on recent outbreaks. Related: New USDA Proposal Will Make Consuming Chicken Much Safer amid Recalls.
The FDA has announced over 20 recalls across the U.S., including food items, cosmetics, drugs, dietary supplements, and medical devices.
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.