Avant Foaming Hand Sanitizer recalled over manufacturing violations

Recall date

July 15, 2022

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Aire-Master of America Inc recalls Avant Foaming Hand Sanitizer, ethanol 62%, a) 18 fl. oz. bottle (530 mL), b) 1000 mL (33.9 fl. oz.) pouch, c) 55 gallon…

Recall number

D-1355-2022

FDA classification

Class II

Brand / firm

Aire-Master of America Inc

Sold / distributed

Florida, Illinois, Iowa, New Jersey

Why it was recalled

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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