Food recall
Vita 360, LLC recall: Brand Name
Vita 360, LLC, of San Juan, PR, recalled Brand Name. The FDA's reason: “FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on December 7, 2023, and the FDA first listed it in its Enforcement Report of January 17, 2024. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class III
It is unlikely to cause harm
Why
See FDA's words below
Status
Terminated
Closed May 1, 2024
The recall
- Company
- Vita 360, LLC (San Juan, PR)
- Reason, in FDA's words
- “FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.”
- Where it was sold
- Domestic distribution only throughout Puerto Rico
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 93627
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-0710-2024 Class III
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
Codes: Manufacturer Lot #2633; Expiration Date: 07/25
Quantity: 1999 units
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of January 17, 2024.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.