CLASS I Food recall · Reported 23 Oct 2024 · FDA Enforcement Report
Rauwolscine Dietary Supplement, Suppress Appetite recalled
Gorilla Mind is recalling Rauwolscine Dietary Supplement, Suppress Appetite, Increased Fat Loss, Increased Energy, distributed nationwide in the US. The recall was initiated on 6 Sep 2024 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0053-2025
- FDA event ID
- 95313
- Recalling firm
- Gorilla Mind, Boise, ID
- Brand
- Gorilla Mind
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 6 Sep 2024
- FDA classified
- 17 Oct 2024
- Reported
- 23 Oct 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Salmonella
- Product category
- Weight Loss Supplements
Timeline
| 6 Sep 2024 | Recall initiated by company | |
| 17 Oct 2024 | Classified by FDA | +41 days |
| 23 Oct 2024 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product was recalled due to the potential for contamination with Salmonella
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
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***".
Where it was distributed
nationwide
Questions about this recall
Why was it recalled?
Product was recalled due to the potential for contamination with Salmonella
Which lots are affected?
Lot Number: 24041003 EXP: 04/2026
Where was it sold?
nationwide
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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