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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, Reumo Flex, and Kuka Flex Recalled for Undeclared Diclofenac

Agency Publication Date: November 29, 2023
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Summary

Botanical Be is recalling Artri King Reforzado con Origa y Omega 3 tablets, Reumo Flex caplets, and Kuka Flex Forte caplets because they contain undeclared diclofenac. Approximately 535 bottles and boxes are affected by this recall. These products are marketed as dietary supplements for joint health but were found to contain diclofenac, a prescription non-steroidal anti-inflammatory drug (NSAID) not listed on the packaging.

Risk

Undeclared diclofenac can cause serious health risks, including gastrointestinal bleeding, heart attack, or stroke. These risks are significantly higher for individuals who already take other NSAIDs or those with pre-existing heart or stomach conditions.

What You Should Do

  1. This recall affects Artri King Reforzado con Origa y Omega 3 (UPC 750103111138), Reumo Flex (UPC 7502214014598), and Kuka Flex Forte (UPC 0736640810265). Identification details including lot numbers and expiration dates are printed on the product packaging.
  2. 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 Botanical Be directly for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

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 King Reforzado con Origa y Omega 3 (100-count bottles)
Variants: Tablets
UPC Codes:
750103111138
Lot Numbers:
35421 (Exp 12/19/2025)

Manufactured by Plantas medicinales de Mexico.

Product: Reumo Flex (30-count boxes)
Variants: Caplets
UPC Codes:
7502214014598
Lot Numbers:
All lots (Exp 10/20/2024)

Manufactured by Grupo Yepenza de Mexico, SA de CV.

Product: Kuka Flex Forte (30-count bottles)
Variants: Caplets
UPC Codes:
0736640810265
Lot Numbers:
All lots (Exp 12/12/2024)

Manufactured by Kukamonga.

Product Images

Image of Artri Ajo Rey

Image of Artri Ajo Rey

Image of Artri Ajo King

Image of Artri Ajo King

Image 1: “Front label, Artri King, 100 tablets”

Image 1: “Front label, Artri King, 100 tablets”

Image 2: “Kuka Flex Forte Bottle, 30 caplets”

Image 2: “Kuka Flex Forte Bottle, 30 caplets”

Image 3: “Front label, Ypenza brand Reumo Flex, 30 caplets”

Image 3: “Front label, Ypenza brand Reumo Flex, 30 caplets”

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93257
Status: Active
Manufacturer: Botanical Be
Sold By: Botanical Be
Manufactured In: Mexico, United States
Units Affected: 2 products (235 bottles; 300 bottles)
Distributed To: Nationwide
Agency Last Updated: January 12, 2024

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) · FDA Press Release (4) · FDA Press Release (5) · 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.