Drug recall
VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and…
FDA recall event 95959 · Class I · Vidaslim Co.
Key facts
| Event ID | 95959 |
|---|---|
| Recall numbers | F-0468-2025 |
| Recalling firm | Vidaslim Co. |
| Product type | Food |
| Products | 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)… |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Due to the presence of Toxic yellow oleander |
| Initiation date | Dec 11, 2024 |
| Report date | Feb 12, 2025 |
| City | San Antonio |
| State | TX |
| Country | United States |
| FEI number | 3031319574 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: