CLASS I Drug recall · Reported 27 Apr 2022 · FDA Enforcement Report

artnaturals hand sanitizer, Scent Free Hand Sanitizer recalled

Virgin Scent is recalling artnaturals hand sanitizer, Scent Free Hand Sanitizer (ethyl alcohol 5%), distributed nationwide in the US. The recall was initiated on 26 Oct 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot: G20127E, G20128A, EXP 5/1/2022;
Quantity recalled47,832 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0782-2022
FDA event ID
88960
Recalling firm
Virgin Scent, Gardena, CA
Classification
Class I
Status
Terminated
Recall initiated
26 Oct 2021
FDA classified
22 Apr 2022
Reported
27 Apr 2022
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Benzene
Drug class
Hand Sanitizer

Timeline

26 Oct 2021Recall initiated by company
22 Apr 2022Classified by FDA+178 days
27 Apr 2022Published in enforcement report+5 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Chemical Contamination: presence of benzene, acetaldehyde, and acetal.

Product as listed by the FDA

artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5

Where it was distributed

Nationwide in the U.S.A

Nationwide

Questions about this recall

Is artnaturals hand sanitizer, Scent Free Hand Sanitizer (ethyl alcohol 5%) recalled?

Yes. Virgin Scent recalled artnaturals hand sanitizer, Scent Free Hand Sanitizer (ethyl alcohol 5%) on 26 Oct 2021. The recall is Class I and its status is Terminated. Recall number D-0782-2022.

Why was it recalled?

Chemical Contamination: presence of benzene, acetaldehyde, and acetal.

Which lots are affected?

Lot: G20127E, G20128A, EXP 5/1/2022;

Where was it sold?

Nationwide in the U.S.A

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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