Wright Medical Technology, Inc. recalls EasyFuse Dynamic Compression System Instrument Pack
- Recall date
- March 10, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0853-2022
- FDA classification
- Class II
- Brand / firm
- Wright Medical Technology, Inc.
- Sold / distributed
- US distribution to Florida, North Carolina, Ohio, and Texas
Why it was recalled
The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
EasyFuse Dynamic Compression System Instrument Pack
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