Tight! Xtreme Reloaded (SAN Corporation) – Unapproved Ingredient (2021)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
SAN Corporation
Lot Codes / Batch Numbers
C1909182 MFG 11-2019 EXP 11-2022
Products Sold
C1909182 MFG 11-2019 EXP 11-2022
SAN Corporation is recalling Tight! Xtreme Reloaded: 120 count capsules (serving size 3 capsules) Ingredients: Evapor8 Total due to FDA inspection found New Dietary Ingredient, Hordenine, in the supplement product.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
FDA inspection found New Dietary Ingredient, Hordenine, in the supplement product.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AR, CA, KY, NV
Page updated: Jan 6, 2026