OSSOS-SANS Reforzado con: Glucosamina Curcuma Ortiga tablets — Class II drug recall D-0558-2024
Ongoing recall by MexHealth LLC, reported 2024-06-26, distributed nationwide. Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofe
| Recall number | D-0558-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MexHealth LLC, La Mesa, CA, United States |
| Recall initiated | 2024-05-22 |
| Classified | 2024-06-17 |
| Reported by FDA | 2024-06-26 |
| Distributed | Nationwide (US) |
| Quantity | 20 bottles |
| Reason classes | undeclared allergen, unapproved product |
| Lot numbers | H29585 |
Product
OSSOS-SANS Reforzado con: Glucosamina Curcuma Ortiga tablets, packaged in a 30-count bottle, DISTRIBUIDOR POR: Naturistas Especializados, Alce Blanco 180-A Fracc. Industrial, Edo. de Mexico C.P. 53370
Reason for recall
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac and methocarbamol,
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-0558-2024. 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.