NCH Life Sciences recalls 2.5 and 55 gallon alcohol hand sanitizers for impurities exceeding safety limits. Consumers should check product labels for NDC codes 55533-524-02 or 55533-524-03.
CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in the product in excess of allowed limits.
NCH Life Sciences is recalling alcohol-based hand sanitizers that contain impurities of acetal and acetaldehyde in excess of allowed limits. This could pose a risk to health if used improperly, though the specific danger is not detailed in the recall.
The product contains impurities of acetal and acetaldehyde in amounts exceeding the allowed limits. These impurities could potentially cause health issues if the product is used as intended, though the specific health risks are not detailed in the recall.
Anyone who owns or uses the recalled hand sanitizers, particularly those with the NDC codes 55533-524-02 or 55533-524-03. The risk is not clearly defined in the recall notice.
Check for the product name 'Alcohol Antiseptic 80% Topical Solution Hand Sanitizer, Non-Sterile Solution' in 2.5 gallon (9,464 ml) or 55 gallon (208,198 ml) bottles. Look for NDC codes 55533-524-02 or 55533-524-03 on the label.
Look for NDC codes 55533-524-02 or 55533-524-03 on the bottle label to confirm if the product is recalled.
The recall states that impurities of acetal and acetaldehyde were found in excess of allowed limits, but the specific health risks are not detailed in the notice.
The recall does not specify a remedy, so there is no action required beyond checking the product labels for the NDC codes.
Check the product label for NDC codes 55533-524-02 or 55533-524-03, which correspond to the 2.5 gallon and 55 gallon bottles.
We’ve drafted a message you can send NCH Life Sciences to request your refund or repair — edit it as you like.
Subject: Recall D-0092-2023 — NCH Life Sciences NCH Life Sciences Hello, I own a NCH Life Sciences that is covered by recall D-0092-2023 from NCH Life Sciences. 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.
