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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

SAN Corporation: Tight! Xtreme Reloaded Recalled Due to Unapproved Dietary Ingredient

Agency Publication Date: June 23, 2021
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Summary

SAN Corporation is recalling 691 units of its dietary supplement, Tight! Xtreme Reloaded (120 count capsules), because it contains Hordenine, a New Dietary Ingredient that has not been properly vetted for safety by the FDA. The product was distributed to customers in California, Arkansas, Kentucky, and Nevada, as well as internationally to Russia, Japan, and Spain. This recall involves specific batches marked with manufacturing date 11-2019 and expiration date 11-2022. Consumers should stop using this supplement and return it to the place of purchase for a full refund.

Risk

The FDA identified Hordenine as a 'New Dietary Ingredient' for which the manufacturer failed to provide evidence of safety. Using products with unvetted ingredients can pose unpredictable health risks, as the safety profile and potential side effects of this specific ingredient have not been officially established for consumer use.

What You Should Do

  1. Identify if you have the affected product by checking the label for 'Tight! Xtreme Reloaded' in 120-count capsule bottles.
  2. Check the bottle for UPC 6072898 12591 4 and lot/batch code C1909182.
  3. Verify the dates printed on the packaging: look for a manufacturing date (MFG) of 11-2019 and an expiration date (EXP) of 11-2022.
  4. Immediately stop using the product if it matches the identified codes and dates.
  5. Return the product to the place of purchase for a full refund or contact SAN Corporation for further instructions.
  6. If you have experienced any adverse health effects from using this supplement, contact your healthcare provider or physician immediately.
  7. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Full refund upon return.

How to: Return to the place of purchase for a full refund or contact the manufacturer for further instructions.

Affected Products

Product: Tight! Xtreme Reloaded (120 count capsules)
UPC Codes:
607289812591
Lot Numbers:
C1909182 (MFG 11-2019 EXP 11-2022)
Date Ranges: Exp 11-2022

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88121
Status: Resolved
Manufacturer: SAN Corporation
Sold By: Retailers in KY, NV, AR, and CA; International retailers in Russia, Japan, and Spain
Manufactured In: United States
Units Affected: 691 units
Distributed To: Kentucky, Nevada, Arkansas, California

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.