The Recall Desk
Agency classClass IOur severity:CriticalFDA (Drugs)·D-0288-2019·Announced 2018-11-21

Euphoric Male Performance Enhancer Recalled for Undeclared Prescription Drugs

Epic Products, LLC is recalling Euphoric Premium Male Performance Enhancer capsules because they contain undeclared sildenafil, tadalafil, and oxytetracycline.

The agency’s classification

FDA (Drugs): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of 5 per the rubric.

Plain-English summary

Epic Products, LLC is recalling Euphoric Premium Male Performance Enhancer capsules. The product is marketed in 1-count blister cards, 3-count bottles, and 12-count bottles. The recall covers all lots of the product.

The FDA has determined that the product contains undeclared sildenafil, tadalafil, and oxytetracycline. These are FDA-approved drug products, which makes Euphoric an unapproved drug marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).

The product was distributed nationwide in the USA. Consumers should stop using the product and contact the manufacturer for instructions on how to return it or obtain a refund.

The recalled product

Product
Euphoric Premium Male Performance Enhancer capsules, packaged in a)1-count blister cards, UPC 6 96859 28646 9, b) 3-count bottle, UPC 6 96859 28647 6 and c) 12-count bottle, UPC 6 96859 28648 3.
Manufacturer
Epic Products, LLC

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • All lots

Distribution

Distributed nationwide across the United States.

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