ALOE GATOR — Class II drug recall D-0530-2024
Ongoing recall by ARG Laboratories, Inc., reported 2024-06-05, distributed nationwide. Out of Specification for active ingredient
| Recall number | D-0530-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ARG Laboratories, Inc., Dallas, TX, United States |
| Recall initiated | 2024-04-17 |
| Classified | 2024-05-30 |
| Reported by FDA | 2024-06-05 |
| Distributed | Nationwide (US) |
| Quantity | 6,264 |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 00017971104217 |
| Lot numbers | 04023C1 |
| Expiration dates | 2025-01-31 |
Product
ALOE GATOR, (Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%), SPF 40+, Broad Spectrum Protective Gel, Sport Performance, NET WT 4 OZ (113g), Manufactured for AGS Brands. UPC 0 17971 10421 7
Reason for recall
Out of Specification for active ingredient
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-0530-2024. 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.