Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Avant Foaming Hand Sanitizer Recalled by Aire-Master of America Inc Due to CGMP Deviations: product manufactured using deionized water from...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aire-Master of America Inc directly.
Affected Products
Avant Foaming Hand Sanitizer, ethanol 62%, a) 18 fl. oz. bottle (530 mL), b) 1000 mL (33.9 fl. oz.) pouch, c) 55 gallon drum, Fragrance Free, Manufactured for B4 Brands, Lisbon, Iowa 62253
Quantity: 18 oz bottle: 11,435 bottles; 1000 mL pouch: 4,116 pouches, c) 2 drums
Why Was This Recalled?
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Where Was This Sold?
Florida, Illinois, Iowa, New Jersey
About Aire-Master of America Inc
Aire-Master of America Inc has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report