FDA Device recall Z-1874-2018
Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)
- FDA Device
- Class II
- terminated
- Published 2018-05-23
On 2018-05-23 the FDA classified a Class II recall of Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002) by Epic Extremity, citing there is an error in the caddy artwork that misidentifies a specific plate and screw.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1874-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-20 |
| Published | 2018-05-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Epic Extremity |
| Distribution | FL, PA, VA |
Product
Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)
Reason
There is an error in the caddy artwork that misidentifies a specific plate and screw.
Identifiers
| code_info | Catalog Number: 2111-0005 Lot: 51464 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1874-2018%22
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