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:
- Online: www.fda.gov/medwatch/report.htm
- Regular mail: Use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to address on the pre-addressed form.
- Fax: 1-800-FDA-0178.
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