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  2. 2010 Johnson & Johnson children's product recall - Wikipedia

    en.wikipedia.org/wiki/2010_Johnson_&_Johnson...

    In Canada, only Children's Motrin and Children's Tylenol Cough & Runny Nose were affected by the recall. [8] According to the FDA, consumers should stop using the recalled products even though the chance of related health problems was "remote." [3] A McNeil spokesperson stated that the recall was not made on "the basis of adverse medical events ...

  3. 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.

  4. 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]

  5. 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 ...

  6. The 28 sodas, juices and other drinks recalled by the FDA ...

    www.aol.com/28-sodas-juices-other-drinks...

    The FDA has recalled 28 beverages so far in 2024, The Daily Mail reported. All but four of the drinks were recalled because they had drugs, bacteria or harmful chemicals in them that the company ...

  7. FDA issues recall for antidepressant drug - AOL

    www.aol.com/fda-issues-recall-antidepressant...

    NEW YORK (PIX11) – The Federal Drug Administration issued a recall on Tuesday for a common medicine for depression. Over 7,000 bottles of Duloxetine were recalled due to the elevated presence of ...

  8. 2022 United States infant formula shortage - Wikipedia

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

    Bare formula shelves with purchase limit notice, at a Safeway store in Monroe, Washington, in January 2022. In 2022, the United States experienced a severe shortage of infant formula as a result of the 2021–2022 global supply chain crisis compounded by a large scale product recall after two babies allegedly died after consuming Abbott infant formula, [1] [2] import restrictions, [3] [4] and ...

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