CLASS I Food recall · Reported 12 Feb 2025 · FDA Enforcement Report

90-day (Original Root, Root Plus, and Root Capsules) recalled

Vidaslim is recalling 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root. The recall was initiated on 11 Dec 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesExpiration date of 12/24 (December 2024) through 12/25 (December 2025)
Quantity recalled760 units

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-0468-2025
FDA event ID
95959
Recalling firm
Vidaslim, San Antonio, TX
Classification
Class I
Status
Terminated
Recall initiated
11 Dec 2024
FDA classified
3 Feb 2025
Reported
12 Feb 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons
Product category
Strawberries

Timeline

11 Dec 2024Recall initiated by company
3 Feb 2025Classified by FDA+54 days
12 Feb 2025Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Due to the presence of Toxic yellow oleander

Product as listed by the FDA

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),

Where it was distributed

These products were sold on a website and through direct sales via independent distributors throughout the USA.

Questions about this recall

Why was it recalled?

Due to the presence of Toxic yellow oleander

Which lots are affected?

Expiration date of 12/24 (December 2024) through 12/25 (December 2025)

Where was it sold?

These products were sold on a website and through direct sales via independent distributors throughout the USA.

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.

Other Strawberries recalls

All 160