Bayer recalls LOTRIMIN AF (Miconazole nitrate 2%) Jock Itch Powder Spray due to potential benzene contamination from manufacturing at a facility with past contamination issues. Affected lots include specific production dates and quantities.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer is recalling certain lots of LOTRIMIN AF Jock Itch Powder Spray because it was manufactured at a facility that previously had benzene contamination. This could pose a risk of serious injury if benzene exposure occurs. Consumers should check their product lot numbers and take appropriate action.
The product was manufactured at a facility that previously had benzene contamination. Benzene is a known carcinogen that can cause serious health issues with prolonged exposure. However, the recall does not specify how the contamination occurred or the actual risk level in this specific product.
People who own or use the recalled LOTRIMIN AF Jock Itch Powder Spray with specific lot numbers listed in the recall notice. Those most at risk are individuals who have used the product in the past few months, especially if they have sensitive skin or use the product frequently.
Check the product label for the lot number (e.g., CV01BEP, CV01D6W, etc.) and the distribution date (e.g., 3/31/2022 to 8/31/2023). The product is a 133g (4.6 oz) can of LOTRIMIN AF Jock Itch Powder Spray from Bayer Healthcare LLC.
Look for the lot number on the product label, such as CV01BEP, CV01D6W, or other specific codes listed in the recall notice.
The recall does not specify if the product is safe to use. It was manufactured at a facility with past benzene contamination, but the exact risk level is not clear.
The recall does not provide specific action steps for consumers. You should check the product lot number and contact Bayer Healthcare for further instructions.
Check the product label for the lot number (e.g., CV01BEP, CV01D6W) and distribution date (e.g., 3/31/2022 to 8/31/2023) as 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-0237-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0237-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
