FDA Drug recall D-1158-2022
Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705
- FDA Drug
- Class II
- completed
- Published 2022-06-22
On 2022-06-22 the FDA classified a Class II recall of Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705 by Walmart, citing marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1158-2022 |
| Classification | Class II |
| Status | completed |
| Initiated | 2022-05-24 |
| Published | 2022-06-22 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Walmart |
| Distribution | US |
Product
Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
Reason
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Identifiers
| upc | 750103112705 |
|---|---|
| code_info | All product lots. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1158-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.