Walmart recalls 100-count Artri King Omega 3 tablets from Mexico due to contamination with undeclared diclofenac, an NSAID. Consumers should check lot numbers and contact Walmart for details.
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.
Walmart is recalling 100-count Artri King Omega 3 tablets from Mexico that contain undeclared diclofenac, a painkiller. This poses a risk of unintended medication interactions or side effects due to the unapproved NSAID.
The tablets contain diclofenac, an NSAID approved for pain and inflammation, but it was not declared on the product label. This could lead to unintended medication interactions or side effects if the product is taken with other pain medications or by people with certain health conditions.
Anyone who purchased the 100-count Artri King Omega 3 tablets from Walmart in Mexico. People taking pain medications or with sensitive health conditions are at slightly higher risk.
Check for the lot number LTARTKNGOMG30720 on the bottle. The product was sold in Mexico with a 100-count bottle, UPC 7 501031 111190, and expires December 2026.
Look for the lot number LTARTKNGOMG30720 on the bottle to confirm if it's recalled.
The product contains undeclared diclofenac, which could cause unintended medication interactions or side effects. Do not take if you have health conditions that require avoiding NSAIDs.
The recall record does not specify a refund or replacement process. Contact Walmart directly for assistance.
Check the lot number on the bottle. If it matches LTARTKNGOMG30720, stop using it and contact Walmart for instructions.
We’ve drafted a message you can send Walmart to request your refund or repair — edit it as you like.
Subject: Recall D-1157-2022 — Walmart Walmart Hello, I own a Walmart that is covered by recall D-1157-2022 from Walmart. 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.
