Recall Radar

Vita 360 recalls Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar…: label issue

January 17, 2024 · Vita 360 Class III

Class IIIFDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.
Reason for the recallFDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Vita 360
Location
San Juan, PR
Reported by FDA
January 17, 2024
Recall started
December 7, 2023
Risk class
Class III
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Supplements and infant formula
Reason type
Labeling and quality

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • 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
    Quantity: 1999 units
    Codes: Manufacturer Lot #2633; Expiration Date: 07/25

Where it was distributed

Domestic distribution only throughout Puerto Rico

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Vita 360 recalled 1 product, including Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose Capsules per bottle.….

Why was it recalled?

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

What does Class III mean?

FDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.

Where was it sold or shipped?

Domestic distribution only throughout Puerto Rico

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

Similar recalls in supplements and infant formula

Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.