Drug recall
Euphoric Premium Male Performance Enhancer capsules, packaged in a)1-count blister cards, UPC 6 96859 28646 9…
FDA recall event 79842 · Class I · Epic Products, LLC
Key facts
| Event ID | 79842 |
|---|---|
| Recall numbers | D-0288-2019 |
| Recalling firm | Epic Products, LLC |
| Product type | Drugs |
| Products | 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. |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Apr 16, 2018 |
| Report date | Nov 21, 2018 |
| Termination date | Oct 3, 2024 |
| City | Overland Park |
| State | KS |
| Country | United States |
| FEI number | 3014364226 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: