Artri Ajo King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico ...

FDA Recall #D-1295-2022 — Class I — May 26, 2022

Recall #D-1295-2022 Date: May 26, 2022 Classification: Class I Status: Terminated

Product Description

Artri Ajo King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO , Melchor Ocampo No. 55 Local D, Delegacion Xochimilco. C.P. 16800, Mexico, D.F., ASIN B092P4615M, UPC 7 501031 111190

Reason for Recall

Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.

Recalling Firm

Amazon.com, Inc. — Seattle, WA

Classification

Class I — Reasonable probability of serious adverse health consequences or death.

Product Type

Drugs

Product Quantity

2,441 bottles

Distribution

Nationwide within the U.S.A.

Code Information

Lot #: LTARTKNGOMG30220, Exp. Diciembre 2025 (December 2025).

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated