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RECALL RECORD — CLASS IIRecall closedD-1355-2022/FDA enforcement
Aire-master of America INC·Cosmetics·Jul 15, 2022

Avant Foaming Hand Sanitizer, Ethanol 62%, a) 18 FL

What you need to know

Class II

  • What happened

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

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Current good manufacturing practice failures can affect product identity, strength, quality or purity.

  • Action required

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Recall closed · classified by the FDADistribution not listedMore cosmetics

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Match before you discard

Product identification

Source: FDA COSMETICS

Brand nameAire-master of America INC
Recalling firmAire-master of America INCNixa, MO, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • [Product number], lot code, expiry: a) [46016] Lot 722770, exp 07/22 b) [46017] Lot 722995-exp 07/22, 727370-exp 07/23, 727898-exp 09/23, 728005-exp 08/23, 729522-exp12/23, 730412-exp 03/24, 730861-exp 04/24 c) [46138] Lot 725188-exp 12/22
Distribution area

Florida, Illinois, Iowa, New Jersey

United States

Quantity affected18 oz bottle: 11, 435 bottles; 1000 mL pouch: 4, 116 pouches, c) 2 drums
Recall initiationFDA report date: August 24, 2022
FDA recall numberD-1355-2022

Beyond the headline

The recall, in context

Aire-master of America INC initiated this cosmetics recall on July 15, 2022. The FDA enforcement report states: CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization. The FDA report lists distribution as: Florida, Illinois, Iowa, New Jersey.

The FDA enforcement report describes the reason as: CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Avant Foaming Hand Sanitizer, Ethanol 62%, a) 18 FL was made or distributed by Aire-master of America INC in Nixa, MO, United States. This page reflects FDA report D-1355-2022, dated August 24, 2022.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, current good manufacturing practice failures can affect product identity, strength, quality or purity.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Set the product aside and do not apply it.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Avant Foaming Hand Sanitizer, Ethanol 62%, a) 18 FL recall?

Aire-master of America INC recalled Avant Foaming Hand Sanitizer, Ethanol 62%, a) 18 FL in an FDA Class II enforcement action reported as D-1355-2022. CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

What should I do if I bought this product?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Aire-master of America INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-1355-2022. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.