Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Oct 26, 2021 (5 years ago)

artnaturals Hand Sanitizer

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

Why it was recalled

CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot

Cause type: cGMP deviation

Departures from current Good Manufacturing Practice found in production or during FDA inspection. A broad quality-system cause: the batch was made under conditions that fall short of FDA manufacturing standards. All cgmp deviation recalls.

What was recalled

artnaturals Hand Sanitizer

Recalling firm
Virgin Scent INC
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0784-2022 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Virgin Scent INC

All 2021 recalls
Class II · Moderate risk

artnaturals hand sanitizer

CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot

Terminated cGMP deviation Virgin Scent INC D-0783-2022

Other cgmp deviation recalls from 2021

All cgmp deviation recalls