Acuity Specialty Products recalls isopropyl alcohol hand sanitizer due to untested alcohol components potentially containing methanol. Affected lots expire by November 2025 and April 2026. Consumers should stop using and contact for details.
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.
Acuity Specialty Products is recalling hand sanitizer products that may contain methanol due to untested alcohol components. This could cause serious health risks if methanol is present. Consumers should stop using these products immediately.
The hand sanitizer was made using alcohol components that weren't tested for methanol. Methanol is toxic and can cause serious health issues if ingested or absorbed through skin.
Hand sanitizer users who purchased the recalled products from the listed lots and expiration dates. People using these products for hand hygiene are most at risk.
Check for lot numbers C2432725 (expires Nov 2025), C2508304 (expires Mar 2026), or C2509304 (expires Apr 2026) on the product label. The product comes in 4x1 gallon cases, 5 gallon pails, or 55 gallon drums.
Immediately stop using the recalled hand sanitizer products as they may contain methanol.
The hand sanitizer may contain methanol, which is toxic and can cause serious health issues if ingested or absorbed through skin.
Check for lot numbers C2432725 (expires Nov 2025), C2508304 (expires Mar 2026), or C2509304 (expires Apr 2026) on the product label.
Contact Acuity Specialty Products at 800-345-1329 or visit their toll-free number for details.
We’ve drafted a message you can send Acuity Specialty Products to request your refund or repair — edit it as you like.
Subject: Recall D-0005-2026 — Acuity Specialty Products Acuity Specialty Products Hello, I own a Acuity Specialty Products that is covered by recall D-0005-2026 from Acuity Specialty Products. 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.
