Voluntary Infants’ TYLENOL Recall
McNeil, the makers of Tylenol, are initiating a voluntary recall as a precaution after receiving a small number of complaints from consumers who reported difficulty using the Infants' TYLENOL® SimpleMeasure™ dosing system. SimpleMeasure™ includes a dosing syringe, which a parent or caregiver inserts into a protective cover, or “flow restrictor,” at the top of the bottle to measure the proper dose. In some cases, the flow restrictor was pushed into the bottle when inserting the syringe. Parents can continue to use Infants’ TYLENOL® provided the flow restrictor at the top of the bottle remains in place. If the flow restrictor is pushed into the bottle, parents and caregivers should not use the product.
This recall is restricted to Infants’ Tylenol Oral Suspension 1oz, in the grape flavor. Lot # BIL0U00, BIL0V00, BIL3500, BJL2D00, BJL2E00, BJL2T00, BJL2U00. UPT Code: 300450122308
Some samples of this product were given to parents at North Central Baptist Hospital and our Stone Oak location during the weeks of 2/6 – 2/17/12. If you have used the sample and have any questions please call the number below. If you have not used the sample yet, please me mindful of the statement above with using the syringe.
If the flow restrictor is pushed into the bottle, the parent or caregiver should not use the product. Consumers can request a refund by visiting www.tylenol.com or contacting McNeil at 1-888-222-6036 (Monday-Friday 8 a.m. to 8 p.m. Eastern Time; Saturday-Sunday 9 a.m. to 5 p.m. Eastern Time)
