Skip to content
Use caution Food recall · FDA · Published June 17, 2021

SAN Corp Recalls Tight! Xtreme Reloaded Due to Hordenine

SAN Corporation recalls 691 units of Tight! Xtreme Reloaded dietary supplement due to the presence of undeclared New Dietary Ingredient, Hordenine.

🇺🇸 FDA recall #F-0704-2021FoodSAN Corporation ›
Take action

Contact the company

Recalling firmSAN Corporation3233 Mission Oaks Blvd Unit K · Camarillo, CA 93012-5138
✎ GovInfoNow plain-language explainer

SAN Corporation is recalling Tight! Xtreme Reloaded, a dietary supplement sold in 120-count capsules. The recall was issued because FDA inspections identified the undeclared New Dietary Ingredient, Hordenine, in the product. This ingredient is listed in the Evapor8 Total Body Fat Assault Matrix formula found within the capsules. Read more at govinfonow.com/recall/14400-san-corp-recalls-tight-xtreme-reloaded-due-to-hordenine.

Source Summary by GovInfoNow · govinfonow.com/recall/14400-san-corp-recalls-tight-xtreme-reloaded-due-to-hordenine · Updated October 10, 2026 · FDA enforcement record: FDA #F-0704-2021

Cite this page

“SAN Corp Recalls Tight! Xtreme Reloaded Due to Hordenine.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/14400-san-corp-recalls-tight-xtreme-reloaded-due-to-hordenine. Based on FDA recall #F-0704-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0704-2021%22&limit=1).

SAN Corporation voluntarily recalled Tight! Xtreme Reloaded Capsules due to the presence of undeclared Hordenine, according to the FDA. The Food and Drug Administration announced the recall on June 17, 2021.

How to tell if you have it

  • Brand: SAN Corporation
  • Product: Tight! Xtreme Reloaded Capsules
  • UPC: 6072898 12591 4
  • Lot Code: C1909182
  • Manufacturing Date: 11-2019
  • Expiration Date: 11-2022

The hazard

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

Context

GovInfoNow's records show SAN Corporation has been subject to other recent recalls of similar products, including A&P Creations Recalls X10 Supplement Due to Undeclared Drugs (2026-09-14), Modern Warrior Dietary Supplement Recall: Unapproved Ingredients Found (2026-01-09), and ZMB Enterprises Addall XR Shot 1 Recall: Contains 1,4-DMAA and Phenylethylamine (2026-04-03).

How to tell if you have this one

Check for the product name Tight! Xtreme Reloaded in 120-count capsules. Look for UPC 6072898 12591 4 and lot code C1909182. The manufacturing date is 11-2019 and the expiration date is 11-2022.

  • Brand
    SAN Corporation
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not consume the Tight! Xtreme Reloaded capsules due to the presence of undeclared Hordenine.

  2. Check your inventory

    Verify if you have units with UPC 6072898 12591 4 and lot code C1909182 manufactured in 11-2019.

Where it went and when

Where it was distributed

Distributed in 4 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “KY, NV, AR and CA and Russia, Japan and Spain.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arkansas, California, Kentucky, Nevada.

Recall timeline

FDA terminated this recall 40 days after the firm started it.

1. Firm started the recall: Jun 17, 202112. FDA classified it Class II: Jun 23, 202123. Published in FDA’s Enforcement Report: Jun 30, 202134. FDA terminated the recall: Jul 27, 202142021
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest food recalls

Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0704-2021 (June 17, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0704-2021 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA