Reported Nov 24, 2021 · Terminated

LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) can, packaged as (a) single…

Bayer Healthcare Pharmaceuticals Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Bayer Healthcare Pharmaceuticals Inc. · 100 Bayer Blvd · Whippany, NJ · 07981-1544

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 byBayer Healthcare LLC, Whippany, NJ 07981, Product of Finland

Lot codes and dates: 8 of 8 products
Products covered by this recall
# Product as published
1 Lot # (a)TN0023C, EXP 1/31/2022
2 TN003C7, EXP 4/30/2022
3 TN00570, EXP 7/31/2022
4 TN0056Z, TN005KJ, EXP 8/31/2022
5 (b)TN0023C, EXP 01/31/2022
6 TN003C7, EXP 04/30/2022
7 TN0023DV, TN0023DAV, TN0023DBV, TN0023DC, EXP 02/28/2022
8 TN005KJ, TN005KJA, TN005KJB, EXP 08/31/2022
Amount recalled: 579,456 cans

The agency filed one notice per product. You are reading one of them; the other 18 are below.

6 more are in the archive.

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

This product could cause temporary or reversible health problems — stop using it.

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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