FDA Device recall Z-0853-2022
EasyFuse Dynamic Compression System Instrument Pack
- FDA Device
- Class II
- terminated
- Published 2022-04-06
On 2022-04-06 the FDA classified a Class II recall of EasyFuse Dynamic Compression System Instrument Pack by Wright Medical Technology, citing the drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0853-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-03-10 |
| Published | 2022-04-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Wright Medical Technology |
| Distribution | FL, NC, OH, TX |
Product
EasyFuse Dynamic Compression System Instrument Pack
Reason
The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
Identifiers
| code_info | Model Number FFSP1530, UDI: 00889797103565 Lot Codes (Expiration Date): 781853-110321 (11/03/2029) and 780395-112221 (12/03/2029) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0853-2022%22
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