Artri King recall
Artri King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO , Melchor Ocampo No.…
Why was Artri King recalled?
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: LTARTKNGOMG30720, Exp. Diciembre 2026 (December 2026)
- Product
- Artri King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO , Melchor Ocampo No.…
- Recalling firm
- Amazon.com, Inc.
- Quantity
- 15,087 bottles
- Distribution
- Nationwide within the U.S.A.
- Recall date
- July 27, 2022
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)