Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets — Class II drug recall D-1158-2022
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-1158-2022 |
|---|---|
| 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 Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
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-1158-2022. 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.