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Wright Medical Technology, Inc. recalls EasyFuse Dynamic Compression System Instrument Pack

Recalled April 6, 2022 · FDA recall Z-0853-2022 · Wright Medical Technology

Hazard
The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking. · FDA Class II
Units
176 packs
Sold at
US distribution to Florida, North Carolina, Ohio, and Texas

Description

The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.

Product
EasyFuse Dynamic Compression System Instrument Pack
Manufacturer(s)
Wright Medical Technology, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Wright Medical Technology, Inc. recalls EasyFuse Dynamic Compression System Instrument Pack | RecallWatchUSA