RecallHawk
Class I Recall

Gorilla Mind Rauwolscine Dietary Supplement, Suppress Appetite, Increased Fat Loss, Increased Energy, dosage 3mg, 90 cap

Gorilla Mind LLC

Summary

The FDA issued a Class I for Gorilla Mind Rauwolscine Dietary Supplement, Suppress Appetite, Increased Fat Lo by Gorilla Mind LLC. Reason: Product was recalled due to the potential for contamination with Salmonella.

Details

Source

Food Recall

External ID

F-0053-2025

Action Date

2024-10-23

Status

Terminated

Category

food

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***".

Lot/Code Info: Lot Number: 24041003 EXP: 04/2026

Quantity Affected: 1348 bottles

Reason for Recall

Product was recalled due to the potential for contamination with Salmonella

Distribution

nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2024-09-06

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Gorilla Mind LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Gorilla Mind LLC have FDA actions?

This is the only FDA action we have on record for Gorilla Mind LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0053-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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