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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 ...
Johnson & Johnson has announced yet another Tylenol recall, and once again, a foul odor is the culprit. McNeil Consumer Healthcare, a division of Johnson & Johnson, announced the recall on Monday ...
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 ...
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 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 ...
The Chicago Tylenol murders were a series of poisoning deaths resulting from drug tampering in the Chicago metropolitan area in 1982. The victims consumed Tylenol-branded acetaminophen capsules that had been laced with potassium cyanide. Seven people died in the original poisonings, and there were several more deaths in subsequent copycat crimes
On this day in economic and business history... 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 ...
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]