PlainRecalls
FDA Drug Critical Class I Terminated

Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray, NET WT 160g (5.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 58720 6, NDC 11523-0010-2.

Reported: November 24, 2021 Initiated: October 1, 2021 #D-0249-2022

Product Description

Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray, NET WT 160g (5.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 58720 6, NDC 11523-0010-2.

Reason for Recall

Chemical Contamination: presence of benzene

Details

Units Affected
579,456 cans
Distribution
Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a variety of retail channels.
Location
Whippany, NJ

Frequently Asked Questions

What product was recalled?
Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray, NET WT 160g (5.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 58720 6, NDC 11523-0010-2.. Recalled by Bayer Healthcare Pharmaceuticals Inc.. Units affected: 579,456 cans.
Why was this product recalled?
Chemical Contamination: presence of benzene
Which agency issued this recall?
This recall was issued by the FDA Drug on November 24, 2021. Severity: Critical. Recall number: D-0249-2022.