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Class ITerminated in FDA datasetRecall initiated Sep 6, 2024

Gorilla Mind Rauwolscine Dietary Supplement, Suppress Appetite, Increased Fat Loss, Increased…

Recalling firm: Gorilla Mind LLC

Why it was recalled

Product was recalled due to the potential for contamination with Salmonella

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 15, 2025.

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Compare the exact product and package details with the label you have.

ProductGorilla Mind Rauwolscine Dietary Supplement, Suppress Appetite, Increased Fat Loss, Increased Energy, dosage 3mg, 90 capsules per bottle, UPC 8 50017 02016 0. Product is manufactured for Gorilla Mind LLC 7154 W. State Street, STE 138, Boise, ID. Product label declares "***Supplement Facts: Rauwolscine Extract***Other Ingredients: Rice Flour, Gelatin (capsule), Silicon Dioxide, and Magnesium Stearate***".
UPC850017020160

FDA code information

Lot Number: 24041003 EXP: 04/2026

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Full FDA record and distribution details

Original product description

Gorilla Mind Rauwolscine Dietary Supplement, Suppress Appetite, Increased Fat Loss, Increased Energy, dosage 3mg, 90 capsules per bottle, UPC 8 50017 02016 0. Product is manufactured for Gorilla Mind LLC 7154 W. State Street, STE 138, Boise, ID. Product label declares "***Supplement Facts: Rauwolscine Extract***Other Ingredients: Rice Flour, Gelatin (capsule), Silicon Dioxide, and Magnesium Stearate***".

Extracted codes and context

TypeCode / valueContext
UPC850017020160, Increased Fat Loss, Increased Energy, dosage 3mg, 90 capsules per bottle, UPC 8 50017 02016 0. Product is manufactured for Gorilla Mind LLC 7154 W. State Street, STE 138, Boise, ID. Product label declares "***Su
lot24041003Lot Number: 24041003 EXP: 04/2026

Original FDA recall reason

Product was recalled due to the potential for contamination with Salmonella

Recall details

Recall number
F-0053-2025
Event ID
95313
FDA status
Terminated
Initiated
Sep 6, 2024
Reported
Oct 23, 2024
Classified
Oct 17, 2024
Terminated
Mar 15, 2025
Quantity
1348 bottles
Location
Boise, ID, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

nationwide

FDA source record · F-0053-2025

Data updated September 16, 2026. View official FDA data ↗

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