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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 Drug
Medications & Supplements/Dietary Supplements

QMart: Male Sexual Enhancement Supplements Recalled for Undeclared Drug Ingredients

Agency Publication Date: May 6, 2021
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Summary

QMart is recalling approximately 1,400 units of several male sexual performance enhancement supplements, including IMPERIAL GOLD 2000, PremierZen Extreme 3000, Burro en Primavera, and Imperial Platinum 2000. FDA analysis found these products contain sildenafil and/or tadalafil, which are the active ingredients in prescription drugs like Viagra and Cialis. These undeclared drug ingredients can pose serious health risks when they interact with other medications. Consumers should stop using these products and contact a healthcare provider for guidance.

Risk

These supplements contain undeclared sildenafil and tadalafil, which can interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. This interaction can be life-threatening for individuals with diabetes, high blood pressure, high cholesterol, or heart disease who take nitrates.

What You Should Do

  1. Immediately check your supplements for the following products: IMPERIAL GOLD 2000 (UPC 718122040702), PremierZen Extreme 3000 (UPC 728175421887), Burro en Primavera (UPC 638632431055), or Imperial Platinum 2000 (UPC 718122040702).
  2. Check the packaging for the code information 'All', as all lots and batches of these specific UPCs are affected by this recall.
  3. Stop using these products immediately and contact your healthcare provider or pharmacist if you have experienced any problems that may be related to taking these supplements.
  4. Return any unused product to the place of purchase for a full refund and contact QMart for further instructions regarding the disposal or return of the items.
  5. Contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

💰Full Refund

Healthcare consultation and product refund.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: IMPERIAL GOLD 2000, Male Sexual Performance Enhancement (1 Capsule)
Model:
D-0368-2021
UPC Codes:
718122040702
Lot Numbers:
All
Product: PremierZen Extreme 3000, Male Sexual Performance Enhancement (1 Capsule)
Model:
D-0369-2021
UPC Codes:
728175421887
Lot Numbers:
All
Product: Burro en Primavera (2 capsules)
Model:
D-0370-2021
UPC Codes:
638632431055
Lot Numbers:
All
Product: Imperial Platinum 2000 (1 capsule)
Model:
D-0371-2021
UPC Codes:
718122040702
Lot Numbers:
All

Product Images

“Imperial Extreme 2000, Male Sexual Performance Enhancement, 1 capsule for 5 days”

“Imperial Extreme 2000, Male Sexual Performance Enhancement, 1 capsule for 5 days”

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87751
Status: Active
Manufacturer: QMart
Manufactured In: United States
Units Affected: 4 products (200 boxes; 500 boxes; 500 boxes; 200 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.