Arti King Refozado con Ortiga y Omega 3 Tablets — Class I drug recall D-1284-2022
Terminated recall by Latin Foods Market, reported 2022-07-20, distributed nationwide. Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofe
| Recall number | D-1284-2022 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Latin Foods Market, San Jose, CA, United States |
| Recall initiated | 2022-06-10 |
| Classified | 2022-07-21 |
| Reported by FDA | 2022-07-20 |
| Terminated | 2024-05-30 |
| Distributed | Nationwide (US) |
| Reason classes | undeclared allergen, unapproved product |
| Lot numbers | 334 |
| Expiration dates | 2025-11-30 |
Product
Arti King Refozado con Ortiga y Omega 3 Tablets, 100-count bottles, Hecho en Mexico por: "PLANTAS MEDICINALES DE MEXICO", Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800 Mexico, UPC 7 501031 111138
Reason for recall
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared 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-1284-2022. 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.