RecallHawk
Class III Recall

Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose Capsu

Vita 360, LLC

Summary

The FDA issued a Class III for Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Pro by Vita 360, LLC. Reason: FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared..

Details

Source

Food Recall

External ID

F-0710-2024

Action Date

2024-01-17

Status

Terminated

Category

food

Product Description

Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose Capsules per bottle. Container description: White Plastic Bottle 300CC with white cap sealed with clear plastic Total Package size: Master Case with 81 Bottles containing 120 capsules each one. Lot no. 2633, Exp. 07/25 Manufactured in the US

Lot/Code Info: Manufacturer Lot #2633; Expiration Date: 07/25

Quantity Affected: 1999 units

Reason for Recall

FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.

Distribution

Domestic distribution only throughout Puerto Rico

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-07

Company

Vita 360, LLC

San Juan, PR

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 26 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Vita 360, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Vita 360, LLC have FDA actions?

This is the only FDA action we have on record for Vita 360, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0710-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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