FDA Recalls artnaturals Scent-Free Hand Sanitizer for Manufacturing Deviations
artnaturals Scent-Free Hand Sanitizer is recalled due to manufacturing process deviations. Approximately 570,268 bottles distributed nationwide are affected.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II recall with no reported illnesses or injuries. The recall is precautionary, based on manufacturing process deviations involving common ingredients.
Plain-English summary
artnaturals Scent-Free Hand Sanitizer (ethyl alcohol 62.5%) distributed by artnaturals, Gardena, California, is subject to an FDA Class II recall affecting 570,268 bottles. The recall stems from manufacturing deviations where other lots were manufactured using common ingredients as a contaminated lot.
Multiple lot numbers (G20109D through G20133A) with expiration dates of May 1, 2022 and August 1, 2022 are affected. The product was distributed nationwide in the United States.
Consumers should immediately stop using this product and check the lot number on their bottle against the recall notice. No illnesses or injuries have been reported in connection with this recall.
The recalled product
- Product
- 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
- Manufacturer
- VIRGIN SCENT INC
- Category
- Drug — Sanitizer
- Hazard
- Affected units
- 570,268
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Lot: G20109D
- G2019E
- G20125E
- G20125F
- G20125D
- G20125A
- G20126C
- G20126A
- G20126D
- G20126B
- G20126E
- G20127C
- G20127B
- G20127D
- G20127A
- G20127F
- G20128B
- G20128C
- G20128D
- G20128E
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by VIRGIN SCENT INC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
Same manufacturer · VIRGIN SCENT INC
See all →- Severeartnaturals Hand Sanitizer Recalled for Benzene and Chemical Contamination
FDA (Drugs) · 2022-04-27
- ModerateHand Sanitizer Recalled Over Manufacturing Quality Deviations
FDA (Drugs) · 2022-04-27
Same hazard · manufacturing deviation
See all →- SevereBaxter Recalls Clindamycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
- HighBaxter Recalls Vancomycin Injection Due to Manufacturing Deviations
FDA (Drugs) · 2026-09-09
- ModerateSynjardy XR Tablets Recalled Due to Manufacturing Deviations
FDA (Drugs) · 2026-07-08
- ModerateDuloxetine delayed-release capsules recalled for N-nitroso impurity contamination
FDA (Drugs) · 2026-05-13
- ModerateFentanyl Citrate Injectable Solution Recalled for cGMP Deviations
FDA (Drugs) · 2026-05-06