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  2. Eye ointments sold at CVS and Walmart recalled due to ...

    www.aol.com/news/eye-ointments-sold-cvs-walmart...

    The recalled products have expiration dates between February 2024 and September 2025, according to the announcement, and are sold in 3.5-gram tubes that come packaged in cardboard boxes.

  3. 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 ...

  4. These Cold & Flu Medicines Contain an Ingredient the FDA ...

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    The U.S. Food and Drug Administration (FDA) announced that it plans to ban products containing phenylephrine, an ingredient found in many over-the-counter (OTC) oral cold and flu medications.

  5. Tylenol (brand) - Wikipedia

    en.wikipedia.org/wiki/Tylenol_(brand)

    The recall came 20 months after McNeil first began receiving and investigating consumer complaints about moldy-smelling bottles of Tylenol Arthritis Relief caplets, according to the U.S. Food and Drug Administration (FDA). The recall included 53 million bottles of over-the-counter products, involving lots in the Americas, the United Arab ...

  6. 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]

  7. FDA Announces Nationwide Eye Drops Recall Due to Fungal ...

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    The company Alcon Laboratories, maker of a popular brand of eye drops, recalled some of its nationwide stock on Dec. 23, after discovering a fungal contamination in one of its products.

  8. 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.

  9. Tylenol maker defeats lawsuit over labeling

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    The maker of Tylenol defeated a lawsuit by consumers who said they were deceived into overpaying for "Rapid Release" gelcaps that did not relieve pain faster than cheaper tablets, including those ...