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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Dietary Supplements

SUPREX Carb & Sugar Block Recalled for Subpotent Chromium Content

Agency Publication Date: January 9, 2024
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Summary

Vita 360, LLC has recalled 1,999 units of SUPREX Carb & Sugar Block because testing by the FDA revealed the product contains significantly less chromium than what is stated on the label. The supplement was found to have only 16% of the declared chromium content. The product is sold in white plastic bottles containing 120 vegetable capsules, and no injuries or illnesses have been reported to date.

Risk

The product is subpotent, meaning it does not provide the nutritional levels of chromium advertised on the packaging. Consumers relying on this supplement for specific dietary or health management may not receive the intended benefits.

What You Should Do

  1. This recall affects SUPREX Carb & Sugar Block dietary supplements (120 capsules) sold in 300cc white plastic bottles with lot number 2633 and an expiration date of 07/25.
  2. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions or concerns.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: SUPREX Carb & Sugar Block (120 vegetable cellulose capsules)by SUPREX Plant Based Nutrition
Variants: 120 Vegetable Cellulose Capsules per bottle
Lot Numbers:
2633 (Exp 07/25)

Quantity: 1999 units; Recall #: F-0710-2024; Container description: White Plastic Bottle 300CC with white cap sealed with clear plastic

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93627
Status: Resolved
Manufacturer: Vita 360, LLC
Sold By: Retailers in Puerto Rico
Manufactured In: United States
Units Affected: 1999 units
Distributed To: Puerto Rico

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.