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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 Ortiga Supplements Recalled for Undeclared Diclofenac

Agency Publication Date: July 19, 2022
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Summary

Amazon.com, Inc. is recalling 53,150 units of Artri King and Ortiga supplements because they contain undeclared diclofenac, a non-steroidal anti-inflammatory drug (NSAID). The recall includes Artri Ajo King and Artri King tablets, as well as Ortiga mas Ajo Rey tablet and capsule cartons, all of which were manufactured in Mexico and sold nationwide on Amazon.com. If you have health concerns after using these products, you should contact your healthcare provider or pharmacist immediately.

Risk

Undeclared diclofenac can cause serious side effects such as heart attack, stroke, and gastrointestinal bleeding, particularly if taken with other NSAIDs or for a long period. Consumers may unknowingly take this prescription-strength medication, which increases the risk of severe drug interactions and liver or kidney damage.

What You Should Do

  1. This recall affects Artri Ajo King Reforzado con Ortiga y Omega 3 (100-count bottles), Ortiga mas Ajo Rey Reforzado con Omega 3, 6 y 9 (cartons containing tablets and capsules), and Artri King Reforzado con Ortiga y Omega 3 (100-count bottles).
  2. Check your packaging for UPC 750103111190 with lots LTARTKNGOMG30220 (Exp. Dec 2025) or LTARTKNGOMG30720 (Exp. Dec 2026), or UPC 3166557819586 with lot 040 19 (Exp. Feb 2025).
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Amazon.com directly for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

💰Option 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
🗑️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 Ajo King Reforzado con Ortiga y Omega 3 (100-count bottle)
Variants: 500 mg, Tablets
Model:
B092P4615M
UPC Codes:
750103111190
Lot Numbers:
LTARTKNGOMG30220 (Exp. Diciembre 2025)

Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO.

Product: Ortiga mas Ajo Rey Reforzado con Omega 3, 6 y 9 (Carton)
Variants: 30 tablets (500 mg), 60 capsules (400 mg)
Model:
B084L2XM3Z
UPC Codes:
3166557819586
Lot Numbers:
040 19 (Exp. 09 FEB 2025)

Hecho en Mexico por: Omega Nutrition.

Product: Artri King Reforzado con Ortiga y Omega 3 (100-count bottle)
Variants: 500 mg, Tablets
Model:
B084KSV12L
UPC Codes:
750103111190
Lot Numbers:
LTARTKNGOMG30720 (Exp. Diciembre 2026)

Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO.

Product Images

Image of Artri Ajo Rey

Image of Artri Ajo Rey

Image of Artri Ajo King

Image of Artri Ajo King

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90627
Status: Resolved
Manufacturer: Amazon.com, Inc.
Sold By: Amazon.com
Manufactured In: Mexico
Units Affected: 3 products (2,441 bottles; 35,622 cartons; 15,087 bottles)
Distributed To: Nationwide
Agency Last Updated: July 27, 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 · FDA Press Release (1) · FDA Press Release (2) · FDA Press Release (3) · 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.