Bayer recalls Tinactin (Tolnaftate 1%) Powder Spray due to benzene contamination from manufacturing at a facility with past contamination issues. Affected lots have specific lot numbers and expiration dates.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer is recalling Tinactin (Tolnaftate 1%) Powder Spray because it was manufactured at a facility that previously had benzene contamination. This could pose a health risk if the product is used as intended.
The product was made at a facility that previously had benzene contamination. Benzene is a known carcinogen, but the risk here is low because the contamination was detected during manufacturing and the product was not used for extended periods.
People who own or use Tinactin Powder Spray with the specific lot numbers and expiration dates listed in the recall notice are affected. Those with sensitive skin or using the product for extended periods may be at slightly higher risk.
Check the product label for lot numbers: CV015YT (exp 10/31/2021), CV01AE7 (exp 2/28/2022), or other listed lot numbers with specific expiration dates. The product is sold in 133g (4.6 oz) cans labeled as Product of Ireland or Finland.
Look for lot numbers such as CV015YT, CV01AE7, or other specific lot numbers listed in the recall notice.
If you have the recalled product, stop using it immediately to avoid potential health risks.
The product was manufactured at a facility with past benzene contamination, but the risk is low. Use only if you have the specific lot numbers listed in the recall notice.
Check the product label for lot numbers like CV015YT (exp 10/31/2021) or other specific lot numbers listed in the recall notice.
Stop using it immediately and contact 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-0245-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0245-2022 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.
