FDA recall record

SAN Tight! Xtreme Reloaded: 120 count capsules recall — FDA F-0704-2021

FDA inspection found New Dietary Ingredient, Hordenine, in the supplement product.

Class IIclassification
F-0704-2021official record ID
Jun 30, 2021report date

Recall record at a glance

Official recordF-0704-2021
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSAN Corporation
Report dateJun 30, 2021
Recall initiation dateJun 17, 2021
Quantity691 units
LocationCamarillo, CA, United States

Official product description

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

Why the product was recalled

FDA inspection found New Dietary Ingredient, Hordenine, in the supplement product.

Distribution information

KY, NV, AR and CA and Russia, Japan and Spain.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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