Bayer recalls LOTRIMIN AF (Tolnaftate 1%) deodorant powder spray due to potential benzene contamination from manufacturing facility issues. Affected products include specific lot numbers and packaging types.
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 because it was manufactured at a facility where other products were found contaminated with benzene. This could pose a health risk if benzene is absorbed through skin contact.
The product was made at a facility that previously had benzene contamination issues. Benzene is a known carcinogen that can be absorbed through skin contact, but the risk is low for most users unless they apply the product frequently or have sensitive skin.
People who own or use the recalled LOTRIMIN AF deodorant powder spray, particularly those with sensitive skin or who apply it frequently. The risk is generally low for most users.
Check for the product name 'LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray' with a 160g (5.6 oz) can. Look for lot numbers like TN0023C, TN003C7, or TN00570 with expiration dates listed in the recall notice.
Identify the product by checking the UPC code (0 41100 58720 6 for single packs) or lot numbers listed in the recall notice.
Reach out to Bayer Healthcare LLC at 1-800-848-8489 for assistance with the recall or to get replacement products.
The product was manufactured at a facility with past benzene contamination issues, but the risk is low for most users. If you have sensitive skin or apply it frequently, you may want to avoid it.
Check the product details and contact Bayer Healthcare LLC at 1-800-848-8489 for instructions on what to do next.
Look for the product name 'LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray' with a 160g (5.6 oz) can and lot numbers like TN0023C, TN003C7, or TN00570.
We’ve drafted a message you can send Bayer to request your refund or repair — edit it as you like.
Subject: Recall D-0240-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0240-2022 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.
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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.
