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

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

    [3] [8] "A vast portion of the [American] children's medicine market" was affected by the recall. [3] 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. Johnson & Johnson Recalls Tylenol Products on Odor Complaints

    www.aol.com/2010/10/19/johnson-johnson-recalls...

    Johnson & Johnson (JNJ) is recalling Tylenol products because of a musty odor, the company's third such recall in 12 months. J&J is yanking a line of Tylenol 8-hour caplets containing 127,728 ...

  4. Johnson & Johnson Recalling 9.3 Million Bottles of Tylenol ...

    www.aol.com/news/2010-11-24-johnson-and-johnson...

    Johnson & Johnson (JNJ) is recalling nearly 9.3 million bottles of of three Tylenol Cold Multi-Symptom liquid products in order to update the product labeling. The pharmaceutical giant's McNeil ...

  5. Johnson & Johnson Expands Recall of Tylenol Arthritis Caplets

    www.aol.com/news/2009-12-29-johnson-and-johnson...

    The U.S. Food and Drug Administration announced on its MedWatch site Monday that Johnson & Johnson (JNJ) is expanding a voluntary recall of Tylenol Arthritis Caplets following consumer reports of ...

  6. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    In others, FDA informs a company of findings that one of its products is defective and suggests or requests a recall. Usually, the company will comply. If the firm does not recall the product, then FDA can seek legal action under the FD&C Act. These include seizure of available product, and/or injunction of the firm, including a court request ...

  7. 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 ...

  8. The Tylenol Recalls, the End of the Jobs Era, and the Dow's ...

    www.aol.com/2013/10/05/the-tylenol-recalls-the...

    Johnson & Johnson initiated one of the largest drug recalls in history on Oct. 5, 1982, when it withdrew Tylenol from the market in response to a rash of murderous package tampering that.

  9. Johnson & Johnson expands Tylenol, Benadryl recall

    www.aol.com/news/2010-06-17-johnson-and-johnson...

    Johnson & Johnson's McNeil Consumer Healthcare has added five lots of its popular over-the-counter drugs, Benadryl and Tylenol, to its recall list and is offering consumers refunds or product coupons.