Aire-Master recalls fragrance-free hand sanitizer due to microbial contamination risks from improper water treatment during manufacturing. Product numbers 46101 (lots 722712-725054) with expiration dates through 2022 are affected.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Aire-Master is recalling fragrance-free hand sanitizer bottles that were manufactured using deionized water without proper microbial controls. This could lead to contamination risks if the product is used without proper safety measures.
The hand sanitizer was made using deionized water from a system that didn't have proper microbial controls after deionization. This could allow harmful bacteria to grow in the product, potentially causing contamination if the sanitizer is used.
Owners of the fragrance-free hand sanitizer bottles with product number 46101 and lots 722712-725054 are affected. People who use hand sanitizer regularly for hygiene purposes are most at risk.
Check for product number 46101 with lots 722712, 724755, or 725054. The product was sold with expiration dates through July 2022, December 2022, or November 2022.
Look for product number 46101 and lots 722712, 724755, or 725054 on the bottle.
The recall states there were microbial control issues during manufacturing, but the official notice does not specify if the product is safe to use.
The recall record does not provide a remedy, so the official notice does not specify any action steps.
Check for product number 46101 with lots 722712, 724755, or 725054 on the bottle.
We’ve drafted a message you can send Aire-Master to request your refund or repair — edit it as you like.
Subject: Recall D-1357-2022 — Aire-Master Aire-Master Hello, I own a Aire-Master that is covered by recall D-1357-2022 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.
