FDA recall Z-0853-2022
Wright Medical Technology, Inc. · Class II · device
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.
Distribution
US distribution to Florida, North Carolina, Ohio, and Texas
Key facts
- Status
- Terminated
- Initiation date
- 2022-03-10
- Report date
- 2022-04-06
- Termination date
- 2026-04-01
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Memphis, TN, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0853-2022