Hand Sanitizer Recalled Over Manufacturing Quality Deviations
VIRGIN SCENT INC has recalled 46,368 bottles of artnaturals Hand Sanitizer nationwide due to manufacturing process deviations. The affected lots were produced using common ingredients from a contaminated batch.
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 hazard is a manufacturing quality deviation involving shared ingredients from a contaminated batch, which constitutes low-risk contamination.
Plain-English summary
VIRGIN SCENT INC is recalling 46,368 bottles of artnaturals Hand Sanitizer distributed nationwide in the United States due to manufacturing process deviations. The recalled product was manufactured using common ingredients from a lot identified as contaminated.
The recall was initiated because other lots were manufactured with the same ingredients as the contaminated batch, creating potential quality concerns. The affected products have lot numbers G20154A and G20155A, with an expiration date of June 1, 2022.
Consumers who have purchased artnaturals Hand Sanitizer with the recalled lot numbers should discontinue use and contact VIRGIN SCENT INC or their retailer for instructions on proper disposal or replacement.
The recalled product
- Product
- artnaturals Hand Sanitizer
- Manufacturer
- VIRGIN SCENT INC
- Category
- Drug — Topical / Hand Sanitizer
- Hazard
- manufacturing-deviation
- contamination
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 (3)
- Lot: G20154A
- G20155A
- EXP 6/1/2022
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- HighBeak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination
FDA (Drugs) · 2026-06-17
- SevereCIMZIA injection recalled due to lack of sterility assurance
FDA (Drugs) · 2026-05-27
- SevereAtomoxetine Capsules Recalled Due to Labeling Mix-Up Error
FDA (Drugs) · 2026-05-27
- LowPrimidone Tablets Recalled Due to Cross-Contamination with Acemetacin
FDA (Drugs) · 2026-05-27