Vidaslim Co. food recall: VidaSlim 90-day
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 95959
- Recall initiated
- Dec 11, 2024
- Classified by FDA
- Feb 3, 2025
- Posted in Enforcement Report
- Feb 12, 2025
- Terminated
- Sep 11, 2026
- Recalling firm
- Vidaslim Co.
- Firm location
- San Antonio, TX, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Due to the presence of Toxic yellow oleander
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Dec 11, 2024. FDA classified it 54 days later, on Feb 3, 2025. Distribution reported by FDA: These products were sold on a website and through direct sales via independent distributors throughout the USA.
Recalled products (1)
F-0468-2025 Class I Terminated
VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and Root Capsules), VidaSlim 7-day Sample Size (Original Root, Root Plus, and Root Capsules), and VidaSlim Hot Body Brew (Strawberry and Peach flavors),
Codes / lots: Expiration date of 12/24 (December 2024) through 12/25 (December 2025)
Quantity: 760 units
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 95959
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.