FDAFDA · Food and drugs·Recall number D-0239-2022
LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 59036 7, NDC 11523-0010-1.
Published November 24, 2021 · Recall initiated: October 1, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Brand
- LOTRIMIN DAILY PREVENTION DEO
- Manufacturer
- Bayer Healthcare Pharmaceuticals Inc.
- Distributor
- Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a variety of retail channels.
- UPC
- 041100590367
- Lot
- Lot # TN005K4, EXP 4/30/2022; TN005K8, EXP 6/30/2022
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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