FDA found Hand Sanitizer LLC's 80% alcohol hand sanitizer contains acetaldehyde above safety limits. Affected batches from June 2020 may cause skin irritation. Consumers should check batch numbers and contact the manufacturer.
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Hand Sanitizer LLC is recalling 12 fl oz alcohol-based hand sanitizers due to FDA findings that they contain acetaldehyde and acetal above specified limits. This could cause skin irritation in some users. The recall affects specific batches produced between June 2020.
The product contains acetaldehyde and acetal above the FDA's specified safety limits. These chemicals can cause skin irritation in some users, though the risk is not severe enough to cause serious injury.
Owners of Hand Sanitizer LLC's 80% alcohol hand sanitizer bottles with batch numbers 100620-128201 to 100620-128212 are affected. People with sensitive skin may experience irritation from the acetaldehyde levels.
Check the batch number on the bottle, which ranges from 100620-128201 to 100620-128212. The product was distributed by Hand Cleansing Gel 850 Kaliste Saloom Rd. Suite 212 Lafayette, LA 70508.
Look for batch numbers 100620-128201 through 100620-128212 on the product label.
FDA analysis found the product contains acetaldehyde and acetal above specified safety limits.
Check the batch number on the bottle. If it's in the range 100620-128201 to 100620-128212, stop using it and contact the manufacturer.
The recall is for potential skin irritation, not serious injury. The hazard level is low risk.
We’ve drafted a message you can send Hand Sanitizer LLC to request your refund or repair — edit it as you like.
Subject: Recall D-1149-2022 — Hand Sanitizer LLC Hand Sanitizer LLC Hello, I own a Hand Sanitizer LLC that is covered by recall D-1149-2022 from Hand Sanitizer LLC. 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.
