Artri King Reforzado con Ortiga Omega 3 Tablets — Class II drug recall D-1159-2022
Completed recall by Walmart Inc, reported 2022-06-22, distributed nationwide. Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
| Recall number | D-1159-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Walmart Inc, Bentonville, AR, United States |
| Recall initiated | 2022-05-24 |
| Classified | 2022-06-24 |
| Reported by FDA | 2022-06-22 |
| Distributed | Nationwide (US) |
| Quantity | 1,308 bottles |
| Reason classes | labeling, unapproved product |
Product
Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles labeled with UPC 7 501031 111190 and UPC 6 09002 40885, and b) 2 pack of 100-count bottles per carton UPC 3 72426 01434
Reason for recall
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
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-1159-2022. 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.