Bayer Healthcare Pharmaceuticals Inc. recalls LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) can, packaged as (a) single pa
Recalled November 24, 2021 · FDA recall D-0240-2022 · Bayer Healthcare Pharmaceuticals
Hazard
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene. · FDA Class II
Units
579,456 cans
Sold at
Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a variety of retail channels.
Description
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Product
LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) can, packaged as (a) single pack, UPC 0 41100 58720 6, NDC 11523-0010-2; (b) 3-pack, UPC 0 41100 58961 3; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland,
Manufacturer(s)
Bayer Healthcare Pharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →