Epic Extremity Plate System — Class II medical device recall Z-1874-2018
Terminated recall by Epic Extremity, LLC, reported 2018-05-23, distributed in FL, PA, VA. There is an error in the caddy artwork that misidentifies a specific plate and screw.
| Recall number | Z-1874-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Epic Extremity, LLC, Cranberry Twp, PA, United States |
| Recall initiated | 2018-03-20 |
| Classified | 2018-05-15 |
| Reported by FDA | 2018-05-23 |
| Terminated | 2019-04-25 |
| Distributed | FL, PA, VA |
| Quantity | 6 units |
| Lot numbers | 51464 |
| Model numbers | 2111-0005 |
Product
Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)
Reason for recall
There is an error in the caddy artwork that misidentifies a specific plate and screw.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1874-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.