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
- Recalling Firm
- Bayer Healthcare Pharmaceuticals Inc.
- 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.
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