Bayer recalls LOTRIMIN AF (Tolnaftate 1%) deodorant powder spray due to benzene contamination at manufacturing facility. Affected lots may pose health risks from benzene exposure.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer is recalling LOTRIMIN AF deodorant powder spray that was manufactured at a facility with benzene contamination issues. This could pose health risks if the product is used.
The product was manufactured at a facility where other lots were found to contain benzene, a known carcinogen. Benzene exposure can cause health issues, including cancer, especially with prolonged use.
People who own or use the recalled LOTRIMIN AF deodorant powder spray from Bayer Healthcare. Those with sensitive skin or who use the product frequently may be at higher risk.
Check for the product name 'LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray' with net weight 133g (4.6 oz). Look for lot numbers TN005K4 (expires 4/30/2022) or TN005K8 (expires 6/30/2022).
Identify the product by checking the lot number and expiration date on the can.
The recall states that the product was manufactured at a facility with benzene contamination issues, so it is not safe to use.
The recall does not specify a remedy, so contact Bayer Healthcare for guidance.
Check for the product name 'LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray' with net weight 133g (4.6 oz) and lot numbers TN005K4 or TN005K8.
We’ve drafted a message you can send Bayer to request your refund or repair — edit it as you like.
Subject: Recall D-0239-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0239-2022 from Bayer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
