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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 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 ...
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 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.
Product recalls are often a terrible situation for both consumers and companies to be in. While consumers are left with faulty -- or possibly fatal -- products, companies incur millions in costs...
3 Recall classes. Toggle Recall classes subsection. 3.1 Class I. 3.2 Class II. ... II and III Drug Recalls. References. Food Drug and Cosmetic Act, ss. 412 and 518,
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 ...
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