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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

Gorilla Mind Rauwolscine Supplements Recalled for Potential Salmonella

Agency Publication Date: October 15, 2024
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Summary

Gorilla Mind LLC is recalling 1,348 bottles of Gorilla Mind Rauwolscine Dietary Supplement because the products may be contaminated with Salmonella. The recall affects 90-capsule bottles (3mg dosage) that were distributed nationwide. No illnesses or injuries have been reported to date in connection with this issue.

Risk

Salmonella can cause serious and sometimes fatal infections, particularly in children, the elderly, or those with weakened immune systems. Symptoms include fever, diarrhea, nausea, vomiting, and abdominal pain; in rare cases, the infection can enter the bloodstream and cause more severe conditions.

What You Should Do

  1. The recalled products are 90-capsule bottles of Gorilla Mind Rauwolscine Dietary Supplement (3mg) with UPC 850017020160, lot number 24041003, and an expiration date of 04/2026.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 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
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Gorilla Mind Rauwolscine Dietary Supplement (90 capsules)
Variants: 3mg
UPC Codes:
850017020160
Lot Numbers:
24041003 (Exp 04/2026)

Product label declares Ingredients: Rauwolscine Extract, Rice Flour, Gelatin (capsule), Silicon Dioxide, and Magnesium Stearate.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95313
Status: Resolved
Manufacturer: Gorilla Mind LLC
Manufactured In: United States
Units Affected: 1348 bottles
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 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.