Bayer Healthcare Pharmaceuticals Inc. recalls Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray, NET WT 160g (5.6 OZ) can, Dist by: Bayer Healthcar…
- Recall date
- October 1, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0249-2022
- FDA classification
- Class I
- Brand / firm
- Bayer Healthcare Pharmaceuticals Inc.
- Sold / distributed
- Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a variety of retail channels.
Why it was recalled
Chemical Contamination: presence of benzene
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
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.
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