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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 ...
Recalls of Tylenol, Motrin and Benadryl might have received the most attention, but they were just part of the story as recalls of over-the-counter (OTC) and prescription drugs quadrupled in 2009 ...
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]
The Food and Drug Administration is reportedly investigating reports of at least 775 serious side effects from drugs recalled by McNeil Consumer Healthcare, a division of Johnson & Johnson ...
The drugs have what is described as a moldy, musty or. Some of the most popular over-the-counter drugs are being recalled due to a foul smell and reports of vomiting, diarrhea and other stomach ...
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.
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.
Johnson and Johnson's McNeil Consumer Healthcare has expanded its recall of its popular over-the-counter drugs Tylenol, Benadryl and Motrin because of a foul odor. Consumers who bought these lots ...