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  2. 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 ...

  3. 2010 Johnson & Johnson children's product recall - Wikipedia

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

    The 2010 Johnson & Johnson children's product recall involved 43 over-the-counter children's medicines announced by McNeil Consumer Healthcare, a subsidiary of Johnson & Johnson, on April 30, 2010. Medications in the recall included liquid versions of Tylenol, Tylenol Plus, Motrin, Zyrtec, and Benadryl. The products were recalled after it was ...

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

    www.aol.com/cold-flu-medicines-contain...

    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. 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 ...

  6. Tylenol, Motrin, Benadryl recalls spur criminal probe ...

    www.aol.com/news/2010-05-27-tylenol-motrin...

    Top Food and Drug Administration officials told a congressional committee today that Johnson & Johnson, the venerable manufacturer of Children's Tylenol, Motrin, Benadryl and other children's ...

  7. 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.

  8. 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 ...

  9. Another Tylenol Recall, Plus Benadryl, Sudafed and Sinutab

    www.aol.com/news/2011-03-30-another-tylenol...

    Johnson and Johnson's McNeil Consumer Healthcare recalled almost 800,000 bottles of Tylenol, Benadryl, Sudafed PE, and Sinutab products in two recalls linked to previous problems for the ...