Device recall
Z-1874-2018: Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with…
FDA device recall · Class II · Epic Extremity, LLC
Key facts
| Recall number (Z-number) | Z-1874-2018 |
|---|---|
| Recall event | 79824 |
| Product | Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002) |
| Product code | HRS |
| Recalling firm | Epic Extremity, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 25, 2019 |
| 510(k) numbers | K153340 |
| FEI number | 3012453147 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database