Bayer recalls Lotrimin AF liquid spray due to benzene contamination from manufacturing at a facility with past contamination issues. Affected lots have specific UPCs and expiration dates.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer is recalling Lotrimin AF (Miconazole nitrate 2%) liquid spray because it was manufactured at a facility that previously had benzene contamination. This could pose a health risk if the product is used.
The product was made at a facility that previously had benzene contamination. Benzene is a known carcinogen, but the risk here is low as the contamination was detected during manufacturing and the product was not used by the public before the recall.
People who own or use Lotrimin AF liquid spray with the specific UPCs and expiration dates listed in the recall notice are affected. Those with sensitive skin or allergies may be at higher risk.
Check for the UPC 0 41100 on the product label. The affected lots have specific expiration dates and lot numbers listed in the recall notice.
Look for the UPC 0 41100 and expiration dates listed in the recall notice to confirm if your product is affected.
The product was manufactured at a facility with past benzene contamination, but the recall is for specific lots. If your product has the listed UPC and expiration dates, it is affected and should be checked.
Check the UPC on the product label. Affected lots have specific expiration dates and lot numbers listed in the recall notice.
The recall does not specify a remedy, so you should check with Bayer Healthcare Pharmaceuticals Inc. 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-0241-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0241-2022 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.
