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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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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Sustain, SCHWINNNG, and Arize Supplements Recalled for Undeclared Drug Ingredients

Agency Publication Date: February 22, 2024
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Summary

Today The World is recalling approximately 24,000 units of Sustain, SCHWINNNG, and Arize Herbal Dietary Supplements because FDA analysis found they contain undeclared tadalafil and nortadalafil. These ingredients are found in FDA-approved prescription drugs for the treatment of male sexual enhancement, making these supplements unapproved drugs that have not been evaluated for safety or effectiveness. The products were distributed nationwide in the United States and are packaged in boxes containing 10 capsules each.

Risk

These undeclared ingredients can interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous or life-threatening levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates and are at higher risk of experiencing these severe interactions.

What You Should Do

  1. This recall involves Sustain, SCHWINNNG, and Arize Herbal Dietary Supplements sold in boxes containing 10 capsules.
  2. Identify if you have the affected products by checking for the following identifiers: Sustain Herbal Dietary Supplement (Lot BTH:230551, Exp. 12.05.2026 and Lot BTH:230571, Exp. 14.05.2026); SCHWINNNG Herbal Dietary Supplement (Lot 2108, Exp. 10/31/2024); and Arize Herbal Dietary Supplement (Lot 2107, Exp. 10/31/2024).
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Today The World directly for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
🗑️Option 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Sustain Herbal Dietary Supplement (10 capsules)by Sustain
Lot Numbers:
BTH:230551 (Exp 12.05.2026)
BTH:230571 (Exp 14.05.2026)

Distributed by VSD Productions, Inc. Las Vegas, Nevada. Recall #: D-0343-2024.

Product: SCHWINNNG Herbal Dietary Supplement (10 capsules)by SCHWINNNG
Lot Numbers:
2108 (Exp 10/31/2024)

Distributed by: Today the World LLC, Vancouver, WA 98683. Recall #: D-0344-2024.

Product: Arize Herbal Dietary Supplement (10 capsules)by Arize
UPC Codes:
721405577477
Lot Numbers:
2107 (Exp 10/31/2024)

Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001. Recall #: D-0345-2024.

Product Images

“Picture of front package, Arize Dietary Supplements capsules”

“Picture of front package, Arize Dietary Supplements capsules”

“Picture of back of package, Arize Dietary Supplements capsules”

“Picture of back of package, Arize Dietary Supplements capsules”

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93941
Status: Active
Manufacturer: Today The World
Sold By: www.getarize.com; VSD Productions, Inc.; Today the World LLC; Natural Herbal Remedies, LLC
Manufactured In: United States, Malaysia
Units Affected: 3 products (7000 boxes; 11500 boxes; 5500 boxes)
Distributed To: Nationwide

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 · FDA Press Release · 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.