Aire-Master of America recalls Protect U Guard Fragrance-Free Hand Sanitizer due to potential microbial contamination from improper water treatment during manufacturing.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Aire-Master of America is recalling Protect U Guard Foaming Hand Sanitizer (1000 mL) because it was made using deionized water without proper microbial controls, which could lead to contamination. This recall is important because contaminated products may pose health risks if used improperly.
The hand sanitizer was produced using deionized water from a system that did not have adequate microbial controls after deionization. This could allow harmful microorganisms to grow in the product, potentially causing infections if the sanitizer is used without proper hygiene.
People who own or use the recalled Protect U Guard Foaming Hand Sanitizer (1000 mL) manufactured for Protect U Guard in Tampa, Florida. Those with frequent hand hygiene needs are at higher risk due to potential microbial contamination.
Check for the product name 'Protect U Guard Foaming Hand Sanitizer', fragrance-free version, 1000 mL (33.9 fl. oz.) per carton, manufactured for Protect U Guard in Tampa, Florida. The product number is 46112 with lots 722782 expiring August 2022.
Verify the product number 46112 and lot number 722782 on the carton.
The recall does not specify if the product is safe to use; it was manufactured with potential microbial contamination risks.
The recall record does not provide a remedy, so no specific action is required beyond checking product details.
Check for the product number 46112 and lot number 722782 on the carton, which was manufactured for Protect U Guard in Tampa, Florida.
We’ve drafted a message you can send Aire-Master of America to request your refund or repair — edit it as you like.
Subject: Recall D-1358-2022 — Aire-Master of America Aire-Master of America Hello, I own a Aire-Master of America that is covered by recall D-1358-2022 from Aire-Master of America. 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.
