Aire-Master of Common Sense Fragrance Free Hand Sanitizer, 250 Gallon Tote, Microbe recall — FDA D-1360-2022
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
Overview of recall records associated with Aire-Master of America Inc., including dates, categories and classifications where available.
Classification mix: Class II: 6.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.
This page summarizes recall records in which the official source identifies Aire-Master of America Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.