CLASS II Drug recall · Reported 22 Jun 2022 · FDA Enforcement Report
Artri Ajo King Reforzado con Ortiga y Omega, Original recalled
Walmart is recalling Artri Ajo King Reforzado con Ortiga y Omega, Original, distributed nationwide in the US. The recall was initiated on 24 May 2022 and the FDA has classified it as Class II.
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-1158-2022
- FDA event ID
- 90359
- Recalling firm
- Walmart, Bentonville, AR
- Classification
- Class II
- 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
- Hidden Drug Ingredients
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: All lots were found to be unapproved drugs based on labeling claims.
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
Where it was distributed
Nationwide in the USA.
Stores named: Walmart
Questions about this recall
Is Artri Ajo King Reforzado con Ortiga y Omega, Original recalled?
Yes. Walmart recalled Artri Ajo King Reforzado con Ortiga y Omega, Original on 24 May 2022. The recall is Class II and its status is Completed. Recall number D-1158-2022.
Why was it recalled?
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Which lots are affected?
All product lots.
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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