SkinGuard 24 All-Day Hand Sanitizer 2 — Class I drug recall D-1571-2020
Terminated recall by SG24 LLC, reported 2020-09-09, distributed nationwide. Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new d
| Recall number | D-1571-2020 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SG24 LLC, Bolingbroke, GA, United States |
| Recall initiated | 2020-08-14 |
| Classified | 2020-09-11 |
| Reported by FDA | 2020-09-09 |
| Terminated | 2023-06-05 |
| Distributed | Nationwide (US) |
| Quantity | 9,600 bottles |
| Reason classes | chemical contamination, labeling, unapproved product |
| UPC / GTIN / UDI-DI | 00793573147103 |
Product
SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147103
Reason for recall
Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1571-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.