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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

Epic Products, LLC: Euphoric Male Performance Capsules Recalled for Undeclared Drugs

Agency Publication Date: November 15, 2018
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Summary

Epic Products, LLC is recalling approximately 244,698 units of Euphoric Premium Male Performance Enhancer capsules because the product contains undeclared sildenafil, tadalafil, and oxytetracycline. These substances are FDA-approved prescription drugs for erectile dysfunction and an antibiotic, respectively, which makes the product an unapproved drug. The recall affects 1-count blister cards, 3-count bottles, and 12-count bottles sold nationwide. Consumers are advised to contact their healthcare provider and return the product to the place of purchase.

Risk

The undeclared sildenafil and tadalafil can interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous or life-threatening levels. The presence of the undeclared antibiotic oxytetracycline also poses a risk of adverse reactions or sensitivity issues for certain users.

What You Should Do

  1. Check your supply for Euphoric Premium Male Performance Enhancer capsules in 1-count blister cards (UPC 6 96859 28646 9), 3-count bottles (UPC 6 96859 28647 6), or 12-count bottles (UPC 6 96859 28648 3).
  2. Confirm if your product is affected by looking for 'All lots' of these specific UPC codes.
  3. Stop using the product immediately as it contains undeclared prescription medications and an antibiotic.
  4. Contact your healthcare provider or pharmacist for guidance if you have consumed this product or have health concerns.
  5. Return any unused product to the pharmacy or place of purchase for a refund.
  6. Contact Epic Products, LLC at their Overland Park, Kansas location for further instructions regarding this recall.
  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

๐Ÿ’ฐFull Refund

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

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

Affected Products

Product: Euphoric Premium Male Performance Enhancer (1-count blister cards)
Model:
Recall #: D-0288-2019
UPC Codes:
696859286469
Lot Numbers:
All lots
Product: Euphoric Premium Male Performance Enhancer (3-count bottle)
Model:
Recall #: D-0288-2019
UPC Codes:
696859286476
Lot Numbers:
All lots
Product: Euphoric Premium Male Performance Enhancer (12-count bottle)
Model:
Recall #: D-0288-2019
UPC Codes:
696859286483
Lot Numbers:
All lots

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79842
Status: Resolved
Manufacturer: Epic Products, LLC
Manufactured In: United States
Units Affected: a) 106,329 cards; b) 109,725 bottles; c) 28,644 bottles
Distributed To: Nationwide
Agency Last Updated: November 30, 2018

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 ยท 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.