Class ITerminatedVoluntary: Firm initiated
Vidaslim Co.: food recall F-0468-2025
Vidaslim Co. of San Antonio, TX recalled VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and Root… Reason: Due to the presence of Toxic yellow oleander. The FDA listed it as Class I in its Enforcement Report dated Feb 12, 2025; distribution: nationwide.
Record status as published: Terminated (terminated Sep 11, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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),
- Product quantity
- 760 units
- Reason for recall
- Due to the presence of Toxic yellow oleander
- Codes, lots and dates on the package
- Expiration date of 12/24 (December 2024) through 12/25 (December 2025)
- Distribution pattern
- These products were sold on a website and through direct sales via independent distributors throughout the USA.
- Recalling firm
- Vidaslim Co., San Antonio, TX
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 11, 2024 |
| Classified by the FDA | Feb 3, 2025 |
| Published in the Enforcement Report | Feb 12, 2025 |
| Terminated | Sep 11, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0468-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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