US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 15, 2022 (4 years ago)

Avant Foaming Hand Sanitizer Ophardt, Fragrance Free, 1000 mL (33.9 fl. oz.) per plastic…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
Aire-Master of America Inc
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1356-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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