A.P. Nonweiler recalls Alcohol Antiseptic 80% hand sanitizer due to FDA-detected acetaldehyde and acetal levels exceeding safety limits. Consumers should check product codes and lot numbers for affected items.
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
A.P. Nonweiler is recalling alcohol antiseptic hand sanitizer products that contain acetaldehyde and acetal levels above FDA safety limits. This could pose a risk of overexposure to these chemicals, though the recall does not specify serious injury or death.
The product contains acetaldehyde and acetal levels that exceed FDA specifications. This could lead to overexposure if the product is used as intended, though the exact health effects are not detailed in the recall.
Anyone who owns or uses the recalled alcohol antiseptic hand sanitizer products. People using the product for hand sanitizing are most at risk due to potential chemical exposure.
Check for product codes: 9999D361-250 (250 gallons) or 9999D361-001 (1 gallon). The lot number 54931 is also associated with this recall. The product has no expiration date.
Look for product codes 9999D361-250 or 9991D361-001 and lot number 54931 to confirm if your item is affected.
The recall states the product contains acetaldehyde and acetal levels above FDA specifications, but does not specify if it is safe to use.
Check for product codes 9999D361-250 (250 gallons) or 9999D361-001 (1 gallon) and lot number 54931.
The recall does not specify a remedy, so the official notice does not state what action to take.
We’ve drafted a message you can send A.P. Nonweiler to request your refund or repair — edit it as you like.
Subject: Recall D-1142-2022 — A.P. Nonweiler A.P. Nonweiler Hello, I own a A.P. Nonweiler that is covered by recall D-1142-2022 from A.P. Nonweiler. 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.
