McNeil Consumer Healthcare Announces Voluntary Nationwide Recall of Infants’ TYLENOL® Oral Suspension, 1 oz. Grape Due to Dosing System Complaints.

No adverse events associated with this action have been reported to date and the risk of a serious adverse medical event is remote. Consumers can continue to use Infants’ TYLENOL® provided the flow restrictor at the top of the bottle remains in place.

Product: Infants’ TYLENOL® Oral Suspension 1oz. Grape

Lot Numbers: BIL0U00, BIL0V00, BIL3500, BJL2D00, BJL2E00, BJL2T00, BJL2U00

UPC Code: 300450122308

Adverse events that may be related to the use of this product may be reported to U.S. Food and Drug Administration’s (FDA) MedWatch Adverse Event Reporting Program either online, by regular mail or by fax:

This voluntary recall is being conducted with the knowledge of the FDA.

CLICK HERE TO SEE FREQUENTLY ASKED QUESTIONS

CLICK HERE TO REQUEST A REFUND

CLICK HERE FOR INFORMATION ON INFANTS’ TYLENOL® SIMPLEMEASURE™

CLICK HERE FOR INFORMATION ABOUT OTHER TYLENOL® RECALLS

For all of the details, click here