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Gorilla Mind LLC Recall: Product was recalled due to the potential for contamination with Salmonella

United States

TerminatedClass I

Company
Gorilla Mind LLC
Product
Gorilla Mind Rauwolscine Dietary Supplement, Suppress Appeti…
Recall date
September 6, 2024
Terminated
March 15, 2025
Source
FDA

Reason for recall

Product was recalled due to the potential for contamination with Salmonella

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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***". Not published in this source record 1348 bottles Lot Number: 24041003 EXP: 04/2026

Distribution

  • nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0053-2025
Event ID
95313
Status
Terminated
Classification
Class I
Company
Gorilla Mind LLC
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***".
Quantity
1348 bottles
Reason
Product was recalled due to the potential for contamination with Salmonella
Recall initiation date
September 6, 2024
Report date
October 23, 2024
Classification date
Not published in this source record
Termination date
March 15, 2025
Distribution pattern
nationwide
UPC, lot, and code information
Lot Number: 24041003 EXP: 04/2026
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Gorilla Mind LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.