FORCE FOREVER 400mg Tablets — Class I drug recall D-0170-2025
Ongoing recall by GNMart LLC, reported 2025-01-08, distributed nationwide. Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexame
| Recall number | D-0170-2025 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GNMart LLC, Dover Plains, NY, United States |
| Recall initiated | 2024-12-12 |
| Classified | 2025-01-02 |
| Reported by FDA | 2025-01-08 |
| Distributed | Nationwide (US) |
| Quantity | 374 bottles |
| Reason classes | unapproved product |
| Expiration dates | 2030-03-27 |
Product
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Reason for recall
Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.
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-0170-2025. 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.