EasyFuse Dynamic Compression System Instrument Pack — Class II medical device recall Z-0853-2022
Terminated recall by Wright Medical Technology, Inc., reported 2022-04-06, distributed in FL, NC, OH, TX. The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
| Recall number | Z-0853-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology, Inc., Memphis, TN, United States |
| Recall initiated | 2022-03-10 |
| Classified | 2022-03-31 |
| Reported by FDA | 2022-04-06 |
| Terminated | 2026-04-01 |
| Distributed | FL, NC, OH, TX |
| Quantity | 176 packages |
| UPC / GTIN / UDI-DI | 00889797103565 |
| Lot numbers | 780395-112221, 781853-110321 |
| Model numbers | FFSP1530 |
Product
EasyFuse Dynamic Compression System Instrument Pack
Reason for recall
The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
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-0853-2022. 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.