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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Artri King and Artri Ajo King Tablets Recalled for Undeclared Diclofenac

Agency Publication Date: June 14, 2022
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Summary

Walmart Inc is recalling approximately 1,308 bottles of Artri King and Artri Ajo King tablets because they were found to contain diclofenac, a prescription-strength anti-inflammatory drug (NSAID) that is not listed on the label. The products were also marketed with unapproved drug claims about treating pain and inflammation. While no injuries have been reported, these tablets were sold nationwide at Walmart locations and online.

Risk

Undeclared diclofenac can cause serious side effects, including gastrointestinal bleeding, heart attack, or stroke, especially if taken with other NSAIDs or by people with certain health conditions. Because the medication is not listed on the label, consumers may accidentally take dangerous amounts of this drug without medical supervision.

What You Should Do

  1. The recalled products are Artri King and Artri Ajo King Reforzado con Ortiga Omega 3 tablets (100-count bottles and 2-packs) with UPC codes 7 501031 111190, 7 501031 12705, 6 09002 40885, and 3 72426 01434.
  2. Check the bottle or carton for lot number LTARTKNGOMG30720 with an expiration date of Diciembre 2026; all other lots of Artri Ajo King and the Artri King 2-pack variants are also included in this recall.
  3. If you have health concerns or believe you have experienced side effects from this product, contact your healthcare provider or pharmacist immediately.
  4. Return any unused product to the place of purchase for a refund, throw it away, or contact Walmart Inc directly for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL (100-count)
Variants: 100-count bottles
UPC Codes:
7501031111190
Lot Numbers:
LTARTKNGOMG30720 (Exp Diciembre 2026)

Quantity: 1,308 bottles total across items

Product: Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL (100-count)
Variants: 100-count bottles
UPC Codes:
750103112705
Lot Numbers:
All product lots
Product: Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL (100-count and 2-pack)
Variants: 100-count bottles, 2-pack of 100-count bottles
UPC Codes:
7501031111190
60900240885
37242601434
Lot Numbers:
All product lots

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90359
Status: Resolved
Manufacturer: Walmart Inc
Sold By: Walmart
Manufactured In: United States, Mexico
Units Affected: 3 products (1308 bottles total)
Distributed To: Nationwide
Agency Last Updated: June 24, 2022

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.