BALTIMORE, MD—Out of an abundance of caution, Johnson & Johnson Consumer Inc. announced on Friday that it would initiate a voluntary recall of a single lot of its Johnson’s Baby Powder in response to a U.S. Food and Drug Administration 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.
JJCI has initiated an investigation into the 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.
JJCI has a rigorous testing standard in place to ensure its cosmetic talc is safe and years of testing, including the FDA’s own testing on prior occasions–and as recently as last month–found no asbestos. Thousands of tests over the past 40 years repeatedly confirm that JJCI consumer talc products do not contain asbestos.
Johnson & Johnson talc comes from ore sources confirmed to meet stringent specifications that exceed industry standards.
If you or someone you provide care for owns a bottle of Johnson’s Baby Powder Lot #22318RB, you are advised to discontinue use of the product. For refund information, contact the Johnson & Johnson Consumer Care Center at www.johnsonsbaby.com or by calling +1 (866) 565-2229.
