FDAFDA · Food and drugs·Recall number D-0240-2022
LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) can, packaged as (a) single pack, UPC 0 41100 58720 6, NDC 11523-0010-2; (b) 3-pack, UPC 0 41100 58961 3; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland,
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
- 041100587206
- Lot
- Lot # (a)TN0023C, EXP 1/31/2022; TN003C7, EXP 4/30/2022; TN00570, EXP 7/31/2022; TN0056Z, TN005KJ, EXP 8/31/2022; (b)TN0023C, EXP 01/31/2022; TN003C7, EXP 04/30/2022; TN0023DV, TN0023DAV, TN0023DBV, TN0023DC, EXP 02/28/2022; TN005KJ, TN005KJA, TN005KJB, EXP 08/31/2022;
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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