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Gorilla Mind Rauwolscine Dietary Supplement recall
Recalled by Gorilla Mind LLC · Boise, ID, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product was recalled due to the potential for contamination with Salmonella
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
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***".
Quantity: 1348 bottles
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot Number: 24041003 EXP: 04/2026
Where it was sold
Nationwide.
FDA's distribution note: nationwide
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Gorilla Mind LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 6, 2024
- In FDA report of
- Oct 23, 2024
- Terminated
- Mar 15, 2025
- FDA recall number
- F-0053-2025 · event 95313
- Official record
- FDA enforcement report search
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