# FDA recall D-0288-2019

> **Epic Products, LLC** · Class I · drug recall initiated 2018-04-16.

## 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.

## Reason for recall

Marketed Without An Approved NDA/ANDA: product contains undeclared sildenafil, tadalafil, and oxytetracycline, FDA approved drug products making Euphoric an unapproved drug.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0288-2019
- **Recalling firm:** Epic Products, LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-04-16
- **Report date:** 2018-11-21
- **Termination date:** 2024-10-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Overland Park, KS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0288-2019

## Citation

> AI Analytics. FDA recall D-0288-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0288-2019. Source: US FDA. Licensed CC0.

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