Johnson & Johnson Consumer Inc. to Voluntarily Recall A Single Lot of Johnson?s Baby Powder in The United States
Company is Acting Out of an Abundance of Caution
Recall Limited to One Lot of Bottles Produced and Shipped in the U.S. in 2018
NEW BRUNSWICK, NJ, October 18, 2019 ? Out of an abundance of caution, Johnson & Johnson Consumer Inc. (JJCI) announced that it is initiating a voluntary recall in the United States of a single lot of its Johnson?s Baby Powder in response to a U.S. Food and Drug Administration (FDA) test indicating the presence of sub-trace levels of chrysotile asbestos contamination (no greater than 0.00002%) in samples from a single bottle purchased from an online retailer. Despite the low levels reported and in full cooperation and collaboration with the FDA, JJCI is initiating this voluntary recall of Lot #22318RB of Johnson?s Baby Powder, from which the tested sample was taken.
In parallel, JJCI has immediately initiated a rigorous, thorough investigation into this matter, and is working with the FDA to determine the integrity of the tested sample, and the validity of the test results. At this early stage of the investigation, JJCI:
- Cannot confirm if cross-contamination of the sample caused a false positive.
- Cannot confirm whether the sample was taken from a bottle with an intact seal or whether the sample was prepared in a controlled environment.
- Cannot confirm whether the tested product is authentic or counterfeit.
- Press Contacts: Ernie Knewitz (732) 524-1090Jake Sargent (202) 569-5086 JSargen3@ITS.JNJ.com Investor Contacts:? Christopher DelOrefice (732) 524-2955 Lisa Romanko (732) 524-2034