Bayer recalls LOTRIMIN AF deodorant spray due to benzene contamination from manufacturing facility issues. Affected lots have specific expiration dates and lot numbers. Consumers should check their product details and contact Bayer for instructions.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer is recalling LOTRIMIN AF deodorant spray products that were manufactured at a facility where benzene contamination was found. This contamination could pose a health risk if the product is used.
The deodorant spray was produced at a facility that previously had benzene contamination issues. Benzene is a known carcinogen that can cause health problems with long-term exposure, but the risk from this specific recall is low due to the small number of affected products and the nature of the contamination.
People who own or use LOTRIMIN AF deodorant spray products with the listed lot numbers and expiration dates are affected. Those with sensitive skin or allergies may be at higher risk.
Check the product label for the lot numbers TN00082, TN000TU, TN000TV, TN00236, TN003C8, TN003C9, TN003GS, TN0041W, TN006W8, TN005P5, or TN006MZ and expiration dates listed above. The product is a 133g (4.6 oz) deodorant powder spray can.
Look for the lot numbers and expiration dates listed in the recall notice to confirm if your product is affected.
The recall notice states that the product was manufactured at a facility with past benzene contamination issues, but the risk is considered low. Bayer recommends checking if your product is affected before using it.
Bayer does not provide specific instructions for affected products in this recall notice. Check the product details to see if it matches the listed lot numbers and expiration dates.
The recall notice does not mention any replacement or refund options. Contact Bayer directly for further assistance.
We’ve drafted a message you can send Bayer to request your refund or repair — edit it as you like.
Subject: Recall D-0236-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0236-2022 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.
