Food recall

SAN Corporation recall: Tight! Xtreme Reloaded

SAN Corporation, of Camarillo, CA, recalled Tight! Xtreme Reloaded. The FDA's reason: “FDA inspection found New Dietary Ingredient, Hordenine, in the supplement product.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on June 17, 2021, and the FDA first listed it in its Enforcement Report of June 30, 2021. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

See FDA's words below

Status

Terminated

Closed July 27, 2021

The recall

Company
SAN Corporation (Camarillo, CA)
Reason, in FDA's words
“FDA inspection found New Dietary Ingredient, Hordenine, in the supplement product.”
Where it was sold
KY, NV, AR and CA and Russia, Japan and Spain.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
88121

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0704-2021 Class II

    Tight! Xtreme Reloaded: 120 count capsules (serving size 3 capsules) Ingredients: Evapor8 Total Body Fat Assault Matrix (Sulbutiamine, Caffeine Anhydrous, Beta-Phenethylamine, Hordeum Vulgare [Root] [Std. to 98% Hordenine], FucoPure [10% Fucoxanthin], Peganum Hamala Extract, Fursultiamine, Citrus Reticulata Extract [Std. to N-Methyltyramine Alkaloid], ChiliMax [Std. to Piperine], Synephrine HCl, Yohimbine HCl). UPC 6072898 12591 4

    Codes: C1909182 MFG 11-2019 EXP 11-2022

    Quantity: 691 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 June 30, 2021.

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.