---
title: "Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. P... — FDA record F-0710-2024 | Is It on Recall"
description: "FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared."
url: https://isitonrecall.com/recall/fda-food-f-0710-2024-brand-name-suprex-plant-based-nutrition-product-name-carb-sugar-block-product-size-120-vegetable-cel/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose Cap... — FDA record F-0710-2024

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 7, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 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
- **Reason**: FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
- **Classification**: Class III
- **Recalling firm**: Vita 360, LLC
- **Quantity**: 1999 units
- **Agency-reported status**: Terminated
- **Source record identifier**: F-0710-2024

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0710-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Manufacturer Lot #2633; Expiration Date: 07/25 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic distribution only throughout Puerto Rico

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jan 17, 2024
- **Recall initiation date**: Dec 7, 2023
- **Center classification date**: Jan 9, 2024
- **Termination date**: May 1, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0710-2024%22)

## Related records

[Other food records](https://isitonrecall.com/category/other-food/) [Vita 360, LLC records](https://isitonrecall.com/brand/vita-360-llc/)