🔍 RecallPedia

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

Class I - Dangerous
Recalled: June 17, 2021 SAN Supplements

What Should You Do?

  1. Check if you have this product:
    C1909182 MFG 11-2019 EXP 11-2022
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
SAN Corporation
Reason for Recall:
FDA inspection found New Dietary Ingredient, Hordenine, in the supplement product.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full 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

Product Codes/Lot Numbers:

C1909182 MFG 11-2019 EXP 11-2022

Distribution:

Distributed in: KY, NV, AR, CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0704-2021

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