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[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."
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 ...
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 ...
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 ...
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 ...
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 ...
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.
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.