CLASS I Drug recall · Reported 20 Jul 2022 · FDA Enforcement Report
Arti King Refozado con Ortiga y Omega, Hecho en Mexico por recalled
Latin Foods Market is recalling Arti King Refozado con Ortiga y Omega, Hecho en Mexico por: "Plantas Medicinales DE, distributed nationwide in the US. The recall was initiated on 10 Jun 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-1284-2022
- FDA event ID
- 90427
- Recalling firm
- Latin Foods Market, San Jose, CA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 10 Jun 2022
- FDA classified
- 21 Jul 2022
- Reported
- 20 Jul 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
Timeline
| 10 Jun 2022 | Recall initiated by company | |
| 20 Jul 2022 | Published in enforcement report | +40 days |
| 21 Jul 2022 | Classified by FDA | +1 day |
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 Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac and dexamethasone.
Product as listed by the FDA
Arti King Refozado con Ortiga y Omega 3 Tablets, 100-count bottles, Hecho en Mexico por: "PLANTAS MEDICINALES DE MEXICO", Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800 Mexico, UPC 7 501031 111138
Where it was distributed
Nationwide in the USA
Questions about this recall
Why was it recalled?
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac and dexamethasone.
Which lots are affected?
Lot 334 21, Exp: 30 Nov, 2025
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.