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  2. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    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.

  3. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    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]

  4. FDA recalls over 7,000 bottles of antidepressant due to possible cancerous chemical. Drew Weisholtz. October 24, 2024 at 1:03 PM. Duloxetine, which can be sold under brand names like Cymbalta, is ...

  5. The FDA Initiated a Class III Recall on More Than 150,000 ...

    www.aol.com/lifestyle/fda-initiated-class-iii...

    The U.S. Food and Drug Administration (FDA) is recalling 151,397.75 bottles of water due to bacterial contamination. According to the FDA's notice, the water was bottled by Berkeley Club Beverages ...

  6. FDA recalls more than 7,000 bottles of antidepressant over a ...

    www.aol.com/fda-recalls-more-7-000-154029555.html

    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 ...

  7. 2022 United States infant formula shortage - Wikipedia

    en.wikipedia.org/wiki/2022_United_States_infant...

    Similac baby formula. The problem was exacerbated when Abbott Labs, one of three major formula producers in the United States, shut down production at its Sturgis, Michigan plant in February 2022, following a Food and Drug Administration recall of several brands of formula due to possible bacterial contamination that may have caused at least two infant deaths. [1]

  8. What You Need to Know About the Recall Affecting Over 4 ...

    www.aol.com/know-recall-affecting-over-4...

    The FDA upgraded the egg recall to class 1 due to a Salmonella outbreak. Here, find a list of the affected eggs and what states have reported illnesses.

  9. MedWatch - Wikipedia

    en.wikipedia.org/wiki/MedWatch

    If a signal is detected, the FDA can issue medical product safety alerts or order product recalls, withdrawals, or labeling changes to protect the public health. Important safety information is disseminated to the medical community and the general public via the MedWatch web site. [5] and the MedWatch E-list. [6]