Bayer recalls LOTRIMIN AF (Miconazole nitrate 2%) Powder Spray due to contamination with benzene at the manufacturing facility. Affected lots have specific expiration dates and packaging details. Consumers should check their product labels and contact Bayer for guidance.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer is recalling LOTRIMIN AF Powder Spray because it was manufactured at a facility that previously had benzene contamination issues. This poses a risk of serious health effects if the product is used. Consumers should stop using the product and contact Bayer for instructions.
The product was made at a facility that previously had contamination with benzene, a known carcinogen. Using this product could expose users to harmful levels of benzene, which may cause serious health issues over time.
People who own or use LOTRIMIN AF Powder Spray with the specific lot numbers and expiration dates listed in the recall notice are affected. Those with the product in their homes or on their person are most at risk.
Check the product label for the lot number and expiration date. The product comes in a 133g (4.6 oz) can with specific packaging details, including NDC numbers and UPC codes. Affected lots have expiration dates from October 2021 to March 2023.
Immediately stop using the recalled LOTRIMIN AF Powder Spray if you have it.
Bayer recalls this product because it was manufactured at a facility that previously had contamination with benzene.
Affected lots include CV017D9 (exp 10/31/2021), CV01940 (exp 11/30/2021), and others with specific expiration dates listed in the recall notice.
Check the product label for the lot number and expiration date. The affected products have specific packaging details, including NDC numbers and UPC codes listed in the recall notice.
We’ve drafted a message you can send Bayer to request your refund or repair — edit it as you like.
Subject: Recall D-0238-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0238-2022 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.
