FDA Drug recall 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 0…
- FDA Drug
- Class II
- terminated
- Published 2021-11-24
On 2021-11-24 the FDA classified a Class II recall of LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 0… by Bayer Healthcare Pharmaceuticals, citing cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0239-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-10-01 |
| Published | 2021-11-24 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Bayer Healthcare Pharmaceuticals |
| Distribution | US |
Product
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.
Reason
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Identifiers
| upc | 041100590367 |
|---|---|
| ndc | 11523-0010-1 |
| ndc | 11523-0010-2 |
| code_info | Lot # TN005K4, EXP 4/30/2022; TN005K8, EXP 6/30/2022 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0239-2022%22
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