Bayer recalls Tinactin (Tolnaftate 1%) Jock Itch Powder Spray due to benzene contamination. Affected units contain lot number TN008M0, expiring April 30, 2023. Consumers should check product details and contact Bayer for guidance.
Chemical Contamination: presence of benzene
Bayer is recalling Tinactin Jock Itch Powder Spray that may contain benzene. This chemical contamination could pose health risks, so affected users should stop using the product and contact Bayer for instructions.
Benzene is a known chemical that can cause health issues when inhaled or absorbed through the skin. The presence of benzene in this product could lead to potential health risks, especially with prolonged use or skin contact.
People who own or use the Tinactin Jock Itch Powder Spray with lot number TN008M0, manufactured in Finland with an expiration date of April 30, 2023, are affected. Those with sensitive skin or using the product for extended periods may be at higher risk.
Check for the product name 'Tinactin (Tolnaftate 1%) JOCK ITCH POWDER SPRAY' with lot number TN008M0 and expiration date April 30, 2023. The product was distributed by Bayer Healthcare LLC in Whippany, New Jersey, and made in Finland.
Look for the lot number TN008M0 and expiration date of April 30, 2023 on the product label.
The recall indicates potential benzene contamination, which could pose health risks. Affected users should stop using the product and contact Bayer for guidance.
Check the product label for lot number TN008M0 and expiration date April 30, 2023. If you have the affected product, stop using it and contact Bayer Healthcare Pharmaceuticals Inc. for instructions.
The recalled product has the lot number TN008M0 and expires April 30, 2023. Check the label for these details to confirm if your product is affected.
We’ve drafted a message you can send Bayer to request your refund or repair — edit it as you like.
Subject: Recall D-0252-2022 — Bayer Bayer Hello, I own a Bayer that is covered by recall D-0252-2022 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.
