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Aire-Master of America Inc recall records

0 reported ongoing

6 records in this archive. Latest source date Jul 15, 2022.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

Records and reported status

FDA drug enforcement

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,...

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

Class IIReported terminated

Distribution: Florida, Illinois, Iowa, New Jersey

Official source
FDA drug enforcement

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.

Class IIReported terminated

Distribution: Florida, Illinois, Iowa, New Jersey

Official source
FDA drug enforcement

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.

Class IIReported terminated

Distribution: Florida, Illinois, Iowa, New Jersey

Official source
FDA drug enforcement

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.

Class IIReported terminated

Distribution: Florida, Illinois, Iowa, New Jersey

Official source

Reasons in these listed records

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

These examples come from this result page and are not a ranking of every recall reason.

Checking Aire-Master of America Inc

Is there a recall on aire-master of america inc right now?

This archive contains 6 records, including 0 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.

Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.

Where can I find older records?

Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

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