CLASS III Food recall · Reported 17 Jan 2024 · FDA Enforcement Report

Suprex Plant Based Nutrition Carb & Sugar Block recalled by Vita 360

Vita 360 is recalling Suprex Plant Based Nutrition Carb & Sugar Block, distributed in Puerto Rico. The recall was initiated on 7 Dec 2023 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesManufacturer Lot #2633; Expiration Date: 07/25
Quantity recalled1999 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0710-2024
FDA event ID
93627
Recalling firm
Vita 360, San Juan, PR
Classification
Class III
Status
Terminated
Recall initiated
7 Dec 2023
FDA classified
9 Jan 2024
Reported
17 Jan 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Potency & Assay
Product category
Plant-Based Meat

Timeline

7 Dec 2023Recall initiated by company
9 Jan 2024Classified by FDA+33 days
17 Jan 2024Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

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

Where it was distributed

Domestic distribution only throughout Puerto Rico

Puerto Rico

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Manufacturer Lot #2633; Expiration Date: 07/25

Where was it sold?

Domestic distribution only throughout Puerto Rico

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other Plant-Based Meat recalls

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