Bayer recalls LOTRIMIN AF (Tolnaftate 1%) deodorant powder spray due to benzene contamination from manufacturing facility. Affected lots contain benzene, a known carcinogen, and may pose health risks with long-term use.
cGMP Deviations: LOTRIMIN AF (Tolnaftate 1%) manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer is recalling LOTRIMIN AF (Tolnaftate 1%) deodorant powder spray because it was manufactured at a facility that previously had benzene contamination. This poses a potential health risk due to benzene, a known carcinogen, especially with long-term use.
The product was manufactured at a facility where other lots were found to contain benzene, a known carcinogen. Benzene exposure can lead to health issues over time, especially with prolonged use of contaminated products.
People who own or use the recalled LOTRIMIN AF deodorant powder spray, particularly those with sensitive skin or long-term users, may be at risk from benzene exposure.
Check for the product name LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray with a net weight of 160g (5.6 oz). The recall includes specific lot numbers and expiration dates listed in the product description.
Identify the product by checking the UPC 041100587206, NDC 11523-0010-2, and lot numbers NAA8997 through NAA9T53 with expiration dates up to 08/31/2022.
The recall indicates potential benzene contamination from the manufacturing facility, which may pose health risks with long-term use. The product is not recommended for use until the recall is addressed.
Check the product details to see if it is in the recalled lots. If it is, contact Bayer Healthcare Pharmaceuticals for further instructions.
Look for the UPC 041100587206, NDC 11523-0010-2, and lot numbers NAA8997 through NAA9T53 with expiration dates up to 08/31/2022.
We’ve drafted a message you can send Bayer to request your refund or repair — edit it as you like.
Subject: Recall D-0254-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0254-2022 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.
