Aire-Master recalls ethanol-based foaming hand sanitizer due to microbial contamination risks from improper water treatment during manufacturing. Products sold in 18 fl oz bottles, 1000 mL pouches, and 55-gallon drums with specific lot numbers are affected.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Aire-Master is recalling ethanol-based foaming hand sanitizers that may contain harmful bacteria due to inadequate microbial controls during manufacturing. This could lead to infections if the sanitizer is used improperly.
The sanitizer was made using deionized water from a system that didn't have proper microbial controls after deionization. This could allow bacteria to grow in the product, potentially causing infections if the sanitizer is used without proper cleaning.
Owners of the recalled hand sanitizers, particularly those using the product for hand hygiene in settings where contamination could cause illness. People with compromised immune systems may be at higher risk.
Check for the product name 'Avant Foaming Hand Sanitizer' with ethanol 62%. Look for specific lot numbers: 722770 (exp 07/22), 722995 (exp 07/22), and other listed lots for each size.
Identify the product by checking the lot number and expiration date on the label.
The product may contain harmful bacteria due to manufacturing issues, so it is not recommended for use until the recall is addressed.
Check the product label for the lot number and expiration date. If it matches the recalled lots, stop using it and contact Aire-Master for instructions.
Look for the lot numbers listed in the recall: 722770 (exp 07/22), 722995 (exp 07/22), and others specific to each size.
We’ve drafted a message you can send Aire-Master to request your refund or repair — edit it as you like.
Subject: Recall D-1355-2022 — Aire-Master Aire-Master Hello, I own a Aire-Master that is covered by recall D-1355-2022 from Aire-Master. 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.
