FDA found Amazon's Artri King Omega 3 tablets contain undeclared diclofenac. Recalled 100-count bottles sold in Mexico with specific lot number. Stop using immediately.
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
Amazon is recalling 100-count bottles of Artri King Omega 3 tablets sold in Mexico because they contain undeclared diclofenac, a painkiller that can cause serious health risks. This product was found to have harmful ingredients not approved for sale in the U.S.
The product contains diclofenac, a nonsteroidal anti-inflammatory drug (NSAID) that can cause serious side effects like stomach bleeding, kidney damage, and heart problems when taken without proper medical supervision. The FDA found this ingredient was not approved for inclusion in the product.
Owners of the recalled 100-count Artri King Omega 3 tablets sold in Mexico with lot number LTARTKNGOMG30720 are affected. People taking these tablets for pain relief are at risk of serious health issues due to the undeclared diclofenac.
Check for the product name 'Artri King Reforzado con Ortiga y Omega 3 tablets', 500 mg, 100-count bottle, manufactured by PLANTAS MEDICINALES DE MEXICO in Mexico. Look for lot number LTARTKNGOMG30720 and expiration date December 2026.
Immediately stop taking the recalled Artri King Omega 3 tablets as they contain undeclared diclofenac which can cause serious health risks.
The FDA found the product contains undeclared diclofenac, a painkiller that can cause serious health risks like stomach bleeding and kidney damage.
Stop using it immediately and contact Amazon for a refund or replacement.
No, the product contains undeclared diclofenac which can cause serious health risks and is not approved for sale in the U.S.
We’ve drafted a message you can send Amazon.com to request your refund or repair — edit it as you like.
Subject: Recall D-1297-2022 — Amazon.com Amazon.com Hello, I own a Amazon.com that is covered by recall D-1297-2022 from Amazon.com. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
