US Drug Recall Register
Class I · High risk Terminated Initiated Oct 1, 2021 (5 years ago)

Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray, NET WT 160g (5.6 OZ)…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Chemical Contamination: presence of benzene

What 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.

Recalling firm
Bayer Healthcare Pharmaceuticals Inc.
NDC code
11523-0010-2
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0249-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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