RecallHawk
Class I Recall

VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and Root Capsu

Vidaslim Co.

Summary

The FDA issued a Class I for VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day ( by Vidaslim Co.. Reason: Due to the presence of Toxic yellow oleander.

Details

Source

Food Recall

External ID

F-0468-2025

Action Date

2025-02-12

Status

Ongoing

Category

food

Product Description

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),

Lot/Code Info: Expiration date of 12/24 (December 2024) through 12/25 (December 2025)

Quantity Affected: 760 units

Reason for Recall

Due to the presence of Toxic yellow oleander

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2024-12-11

Company

Vidaslim Co.

San Antonio, TX

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Vidaslim Co.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Vidaslim Co. have FDA actions?

This is the only FDA action we have on record for Vidaslim Co. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0468-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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