Bayer recalls Lotrimin AF (Tolnaftate 1%) deodorant powder spray due to benzene contamination. Affected units contain specific lot numbers and expiration dates. Consumers should stop using and contact Bayer for details.
Chemical Contamination: presence of benzene
Bayer is recalling Lotrimin AF deodorant powder spray because it contains benzene, a chemical known to be harmful. This recall affects specific lot numbers with expiration dates up to February 2022. Using this product could pose health risks, so affected consumers should stop using it immediately.
Benzene is a known carcinogen and can cause health issues when inhaled or absorbed through the skin. The presence of benzene in Lotrimin AF deodorant powder spray creates a risk of exposure, especially during use, which could lead to serious health effects over time.
People who own or use Lotrimin AF deodorant powder spray with the specific lot numbers TN0023D (expiring February 28, 2022) or TN004BX (expiring June 30, 2022) are affected. Those using the product for skin care or deodorant purposes are at risk of exposure to benzene.
Check the product label for the lot numbers TN0023D (expiring 2/28/2022) or TN004BX (expiring 6/30/2022). The product is a 160g (5.6 oz) deodorant powder spray from Bayer Healthcare.
Immediately stop using Lotrimin AF deodorant powder spray with the affected lot numbers.
The affected lot numbers are TN0023D (expiring February 28, 2022) and TN004BX (expiring June 30, 2022).
Check the product label for the lot numbers TN0023D or TN004BX. The product is a 160g (5.6 oz) deodorant powder spray from Bayer Healthcare.
Stop using it immediately and contact Bayer Healthcare for further instructions.
We’ve drafted a message you can send Bayer to request your refund or repair — edit it as you like.
Subject: Recall D-0249-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0249-2022 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.
