AAFES RECALL  NO. 09-089 RELEASE DATE: 24 September, 2009 SUBJECT: QA PRODUCT WITHDRAWAL INFORMATION – CHILDREN’S AND INFANTS TYLENOL LIQUID PRODUCTS

SCOPE: WORLDWIDE In cooperation with the U.S. Food and Drug Administration (FDA), Johnson & Johnson is withdrawing certain lots of Children's and Infants' TYLENOL® liquid products because an inactive raw ingredient did not meet internal testing requirements. The finished product meets all specifications. NAME OF PRODUCTS: Certain lots of various Children's and Infants' TYLENOL® liquid products that were manufactured between April, 2008 and June, 2008. AAFES only sold the products listed below. INCIDENTS/INJURIES: There have been no incidents reported to date. PRODUCT INFORMATION: UPC ITEM CODE LOT #'S DESCRIPTION 300450186157 1861500 SBM065, SCM005, SCM006, SDM032 Infant's Tylenol Suspension 1/2oz. Cherry 300450247049 2470400 SCM017 Children's Tylenol Plus Cough/ST Suspension 4oz. Cherry 300450249043 2490400 SBM069, SBM070, SCM081, SDM006 Children's Tylenol Plus Cough & Runny Nose 4oz. Cherry 300450407047 4070400 SBM043, SBM044, SCM029 Children's Tylenol Suspension 4oz. Bubble Gum 300450493040 4930400 SBM045, SCM011, SCM030, SDM035 Children's Tylenol Suspension 4oz. Strawberry CONSUMER INFO: Consumers with questions or in possession of the affected products may contact the McNeil Consumer Call Care Center for guidance. Call 1-800-962-5357 (available Monday-Friday 8 a.m. to 8 p.m. Eastern Time). Parents and caregivers who have given the products to their child or infant and have concerns should contact their child's health care provider. Home | History | About AAFES | Store Locator Contact AAFES | Employment | AAFES Sale Flyers | Online Shopping