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
Reported: July 27, 2022 Initiated: May 26, 2022 #D-1297-2022
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
Reason for Recall
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
Details
- Recalling Firm
- Amazon.com, Inc.
- Units Affected
- 15,087 bottles
- Distribution
- Nationwide within the U.S.A.
- Location
- Seattle, WA
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Amazon.com, Inc.. Units affected: 15,087 bottles.
Why was this product recalled? ▼
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 27, 2022. Severity: Critical. Recall number: D-1297-2022.
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