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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 Food
Food & Beverages/Dietary Supplements

Nut Diet Max Nuez de la India Recalled for Toxic Yellow Oleander Substitution

Agency Publication Date: September 19, 2023
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Summary

OBC GROUP CORP is recalling Nut Diet Max Nuez de la India products, including 'LA ORIGINAL - THE ORIGINAL' and 30-capsule bottles. These products were found to contain Yellow Oleander instead of the labeled Aleurites Moluccanus (Nuez de la India). No incidents or injuries have been reported to date, but the substitution poses a severe health risk.

Risk

Yellow Oleander is a highly poisonous plant that contains toxic cardiac glycosides. Ingesting it can lead to severe gastrointestinal distress, irregular heartbeats, and potentially fatal cardiac events.

What You Should Do

  1. This recall affects 'LA ORIGINAL - THE ORIGINAL' Nut Diet Max Nuez de la India with an expiration date in 2024, and Nut Diet Max Nuez de la India 30-capsule bottles (500mg) with an expiration date of 11/2025.
  2. Check your product packaging for the expiration dates '2024' or '11/2025' to determine if your supplement is part of this recall.
  3. Return the product to the place of purchase for a full refund, throw it away, or contact OBC GROUP CORP for further instructions.
  4. If you have consumed these products and experience symptoms like nausea, vomiting, dizziness, or heart palpitations, contact a healthcare provider immediately.
  5. For additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
🗑️Option 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: LA ORIGINAL - THE ORIGINAL, NUT DIET MAX, Nuez de la India
Date Ranges: Exp. Date 2024

Product appears to be Yellow Oleander instead of Nuez de la India as labeled.

Product: NUT DIET MAX, Nuez de la India, Aleurites Moluccanus
Variants: 30 Capsules, 500mg Veggie Caps
Date Ranges: Exp. Date 11/2025

Product appears to be Yellow Oleander instead of Nuez de la India as labeled.

Product Images

Image 1 “Front label, NUT DIET MAX, Neuz de la India”

Image 1 “Front label, NUT DIET MAX, Neuz de la India”

Image 2 “Back clear label showing the seeds”

Image 2 “Back clear label showing the seeds”

Image 3 “NUT DIET MAX, Nuez de la India, 30 capsule container”

Image 3 “NUT DIET MAX, Nuez de la India, 30 capsule container”

“Front label, NUT DIET MAX, Neuz de la India”

“Front label, NUT DIET MAX, Neuz de la India”

“Back clear label showing the seeds”

“Back clear label showing the seeds”

“NUT DIET MAX, Nuez de la India, 30 capsule container”

“NUT DIET MAX, Nuez de la India, 30 capsule container”

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92919
Status: Resolved
Manufacturer: OBC GROUP CORP
Manufactured In: United States
Units Affected: 2 products (Unknown; Unknown)
Distributed To: Nationwide

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) · 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.