Aire-Master of America Inc Recalls

FDA
6
Total Recalls
1
Agencies
Aug 2022
First Recall
Aug 2022
Latest Recall
Sort: Newest first Highest severity

Showing 1-6 of 6 recalls

FDA

Common Sense Fragrance Free Hand Sanitizer, 250 Gallon Tote, Microbe Solutions, LLC, 344-5 Route 9, Suite 237, Lanoka Harbor, NJ 08734

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

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

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

Protect U Guard Foaming Hand Sanitizer, Fragrance Free, 18 fl/oz. (530 mL) per bottle, Manufactured for Protect U Guard, Tampa, FL 33606

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

Avant Foaming Hand Sanitizer Ophardt, Fragrance Free, 1000 mL (33.9 fl. oz.) per plastic carton, Manufactured for B4 Brands, Lisbon, Iowa 52253

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

Protect U Guard Foaming Hand Sanitizer Ophardt, Fragrance Free, 1000 mL (33.9 fl. oz.) per carton, Manufactured for Protect U Guard, Tampa 33606.

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

Stage 2-Ophardt Foaming Hand Sanitizer, Fragrance-Free, 1000 mL (33.9 fl. oz.) per bottle, Manufactured for 2XL Corporation, 2 Gateway Ct, Ste A, Bolingbrook, IL 60440

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