Integrity Biochem recalls lemon-scented hand sanitizer with acetal and acetaldehyde above USP limits. Consumers should check NDC 77512-044-03 and lot 2133607.
CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.
Integrity Biochem is recalling lemon-scented hand sanitizer due to third-party tests finding acetal and acetaldehyde levels exceeding USP standards. This could pose a risk of skin irritation or other adverse reactions if used regularly.
The hand sanitizer contains acetal and acetaldehyde at levels above the USP specifications. These chemicals can cause skin irritation or allergic reactions in some users, especially those with sensitive skin.
Anyone who owns or uses the recalled hand sanitizer, particularly those with sensitive skin who may experience irritation from the chemical contaminants.
Check for the product name 'Integrity Biochem HSC 70-LM, Alcohol Antiseptic 70%, Hand Sanitizer, Lemon Scented Topical Gel' with NDC 77512-044-03 and lot number 2133607. The product was made in the USA on November 23, 2021.
Look for NDC 77512-044-03 and lot number 2133607 on the product label.
The product has been found to contain acetal and acetaldehyde above USP limits, which may cause skin irritation. It is recommended to stop using and check for the recall.
Check for NDC 77512-044-03 and lot number 2133607 on the product label. The product was made in the USA on November 23, 2021.
The recall does not specify a remedy, so you should check with the manufacturer or contact the FDA for further instructions.
We’ve drafted a message you can send Integrity Biochem to request your refund or repair — edit it as you like.
Subject: Recall D-0109-2024 — Integrity Biochem Integrity Biochem Hello, I own a Integrity Biochem that is covered by recall D-0109-2024 from Integrity Biochem. 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.
