Recall: Grape-flavored Infants’ Tylenol—Faulty dosing device
Some 574,000 bottles of grape-flavored liquid Infants Tylenol (1 ounce) have been recalled by Johnson Johnson because reports that the protective cover on the bottles are not working correctly.
Johnson Johnsons McNeil Consumer Healthcare unit has received complaints of difficulty with the Infants Tylenol Simple Measure dosing system, which is inserted into a protective cover at the top of the bottle to measure the proper dose. In some cases, the flow restrictor was pushed into the bottle when the syringe was inserted.
Distributed nationwide, the recalled Infants Tylenol is an over-the-counter product sold as a pain reliever and fever reducer. According to news reports, the bottle is a redesign that was introduced three months ago and was described as a safety improvement to make measuring doses easier.
Recalled bottles have UPC code 300450122308, and include the following lot numbers: BIL0U00, BIL0V00, BIL3500, BJL2D00, BJL2E00, BJL2T00, and BJL2U00.
You can request a refund at www.tylenol.com, or call McNeil at 888-222-6036 (Monday-Friday 8 am to 8 pm ET; Saturday-Sunday 9 am to 5 pm ET).
Childrens Tylenol products are intended for children two years of age and older. To date, no adverse events associated with the recall have been reported. If you have health questions or concerns call your healthcare provider and visit www.tylenol.com for more information.
JJ consumer health segment recalls infant Tylenol [Associated Press]
McNeil Consumer Healthcare Announces Voluntary Nationwide Recall of Infants TYLENOL Oral Suspension, 1 oz. Grape Due to Dosing System Complaints [FDA]