Aroma Release Technologies Inc recalls Klean Touch Hand Sanitizer (70% ethanol) due to unapproved methanol content. This product is marketed without FDA approval as a drug, posing health risks. Consumers should check lot numbers and contact the company for details.
Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol
Aroma Release Technologies Inc. is recalling Klean Touch Hand Sanitizer products that contain methanol, an unapproved drug ingredient. This poses health risks because methanol is toxic and the product lacks FDA approval.
The product is marketed without FDA approval as a drug and contains methanol, which is toxic. Methanol can cause serious health issues if ingested or absorbed through the skin. The unapproved status means it does not meet safety standards for consumer products.
Anyone who owns or uses Klean Touch Hand Sanitizer in 55-gallon drums with specific lot numbers. People using these products for hand sanitizing are at risk due to the unapproved methanol content.
Check for lot numbers 1620-1, 1620-3, 1620-4, 1820-4, 1820-5, 1920-1, or 1920-2 on 55-gallon drums of Klean Touch Hand Sanitizer. The product is sold by Aroma Release Technologies Inc. in Chattanooga, TN.
Look for lot numbers 1620-1, 1620-3, 1620-4, 1820-4, 1820-5, 1920-1, or 1920-2 on the 55-gallon drums.
The product is marketed without FDA approval as a drug and contains methanol, which is toxic. It is not safe for regular use.
The recall record does not specify a remedy, so contact Aroma Release Technologies Inc. at 7026 Discovery Drive, Chattanooga, TN 37416 for further instructions.
Check for lot numbers 1620-1, 1620-3, 1620-4, 1820-4, 1820-5, 1920-1, or 1920-2 on 55-gallon drums of Klean Touch Hand Sanitizer.
We’ve drafted a message you can send Aroma Release to request your refund or repair — edit it as you like.
Subject: Recall D-0298-2022 — Aroma Release Aroma Release Hello, I own a Aroma Release that is covered by recall D-0298-2022 from Aroma Release. 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.
