Pain Wizard — Class II drug recall D-0520-2024
Ongoing recall by ARG Laboratories, Inc., reported 2024-06-05, distributed nationwide. Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing
| Recall number | D-0520-2024 |
|---|---|
| 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 | 3,440 |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 00863865000123 |
| Lot numbers | 18723C3 |
| Expiration dates | 2025-06-30 |
Product
Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Bottle with pump, NET WT 16 fluid oz / 473.17 ml, Made in USA, www.painwizard.com Pain Wizard LLC.PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00012 3
Reason for recall
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
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-0520-2024. 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.