Drug Information Update- FDA Informs Consumers of a Nationwide Voluntary Recall of Certain Tylenol Products

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Title: Drug Information Update- FDA Informs Consumers of a Nationwide Voluntary Recall of Certain Tylenol Products

FDA/CDER/Division of Drug Information (DDI)

The Division of Drug Information (DDI) is CDER's focal point for public inquiries. We serve the public by providing information on human drug products and drug product regulation by FDA. 

The U. S. Food and Drug Administration wants to make consumers aware of a voluntary recall conducted by McNeil Consumer Healthcare of certain lots of oral suspension Children's and Infants' TYLENOL products. This recall was done as a precautionary measure because of potential manufacturing problems. The voluntary recall does not include other Tylenol products.

For more information, please visit: Tylenol Recall


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