Aire-Master recalls fragrance-free foaming hand sanitizer due to microbial contamination risks from improper water treatment during manufacturing. Product may contain harmful bacteria.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Aire-Master is recalling fragrance-free foaming hand sanitizer that was manufactured using deionized water without proper microbial controls. This could lead to harmful bacteria growth in the product, making it unsafe for use.
The hand sanitizer was made using deionized water from a system that didn't have proper microbial controls after deionization. This means harmful bacteria could grow in the product, especially if it's left out for long periods.
People who purchased the specific fragrance-free foaming hand sanitizer with the product number 46076 and lot numbers 722896 or 722996 (expiring July 2022) are affected. Those using this product for hand hygiene are at risk of potential bacterial contamination.
Check for the product name 'Avant Foaming Hand Sanitizer Ophardt, Fragrance Free', 1000 mL (33.9 fl. oz.) in a plastic carton. Look for product number 46076 and lot numbers 722896 or 722996 (expiring July 2022).
Verify the product number (46076) and lot numbers (722896 or 722996) on the plastic carton.
The recall indicates potential microbial contamination risks, so it is not recommended for use until the product is replaced.
The official recall does not specify a remedy, so you should check with Aire-Master of America Inc for further instructions.
Look for the product name 'Avant Foaming Hand Sanitizer Ophardt, Fragrance Free', 1000 mL (33.9 fl. oz.) in a plastic carton with product number 46076 and lot numbers 722896 or 722996 (expiring July 2022).
We’ve drafted a message you can send Aire-Master to request your refund or repair — edit it as you like.
Subject: Recall D-1356-2022 — Aire-Master Aire-Master Hello, I own a Aire-Master that is covered by recall D-1356-2022 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.
