Wrights Lane Synthes USA Products LLC
FDA adverse event reports naming Wrights Lane Synthes USA Products LLC as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: WRIGHTS LANE SYNTHES USA PRODUCTS LLC.
- Total reports
- 26,548
- Deaths
- 4
- Injuries
- 13,760
- Malfunctions
- 12,784
Reports per year
114
26117
4,47418
6,14719
5,42920
7,01221
3,20922
1023
424
125
Source: FDA adverse event reports by year received, 2014–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Screw, Fixation, BoneHWC6,223
- Rod, Fixation, Intramedullary And AccessoriesHSB2,604
- Orthopedic Manual Surgical InstrumentLXH2,371
- ScrewdriverHXX2,339
- Plate, Fixation, BoneHRS2,205
- Guide, Surgical, InstrumentFZX1,212
- Gauge, DepthHTJ943
- ReamerHTO777
- Appliance, Fixation, Nail/Blade/Plate Combination, Multiple ComponentKTT672
- Nail, Fixation, BoneJDS633
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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