CLASS I Drug recall · Reported 22 Jun 2022 · FDA Enforcement Report
Artri King Reforzado con Ortiga Omega, Original recalled by Walmart
Walmart is recalling Artri King Reforzado con Ortiga Omega, Original, Melchor Ocampo No. 55 Local D, distributed nationwide in the US. The recall was initiated on 24 May 2022 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1157-2022
- FDA event ID
- 90359
- Recalling firm
- Walmart, Bentonville, AR
- Classification
- Class I
- Status
- Completed
- Recall initiated
- 24 May 2022
- FDA classified
- 24 Jun 2022
- Reported
- 22 Jun 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Labeling Errors
Timeline
| 24 May 2022 | Recall initiated by company | |
| 22 Jun 2022 | Published in enforcement report | +29 days |
| 24 Jun 2022 | Classified by FDA | +2 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.
Product as listed by the FDA
Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.
Where it was distributed
Nationwide in the USA.
Stores named: Walmart
Questions about this recall
Why was it recalled?
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.
Which lots are affected?
Lot: LTARTKNGOMG30720, Exp Diciembre 2026
Where was it sold?
Nationwide in the USA.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
2 other products · FDA event 90359This product is part of a recall event; the main page for the event is Artri Ajo King Reforzado con Ortiga y Omega, Original recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Artri Ajo King Reforzado con Ortiga y Omega, Original recalled | Walmart | Hidden Drug Ingredients | Nationwide | |
| CLASS II | Artri King Reforzado con Ortiga Omega, Original, a) bottles labeled recalled | Walmart | Hidden Drug Ingredients | Nationwide |
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