Amazon.com, Inc.: Drug Recall

Recall #D-1297-2022 · 05/26/2022

Class I: Dangerous

Recall Details

Recall Number
D-1297-2022
Classification
Class I
Product Type
Drug
Recalling Firm
Amazon.com, Inc.
Status
Terminated
Date Initiated
05/26/2022
Location
Seattle, WA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
15,087 bottles

Reason for Recall

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

Product Description

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. 55 Local D, Delegacion Xochimilco. C.P. 16800, Mexico, D.F., ASIN B084KSV12L, UPC 7 501031 111190

Distribution Pattern

Nationwide within the U.S.A.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.