Stryker Spine-france
FDA adverse event reports naming Stryker Spine-france as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER SPINE-FRANCE.
- Total reports
- 2,526
- Deaths
- 0
- Injuries
- 504
- Malfunctions
- 2,022
Reports per year
49213
53514
55115
48416
42717
3118
220
122
123
224
Source: FDA adverse event reports by year received, 2013–2024. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Orthopedic Manual Surgical InstrumentLXH965
- Appliance, Fixation, Spinal InterlaminalKWP312
- Appliance, Fixation, Spinal Intervertebral BodyKWQ272
- Orthosis, Spondylolisthesis Spinal FixationMNH226
- Thoracolumbosacral Pedicle Screw SystemNKB223
- Intervertebral Fusion Device With Bone Graft, LumbarMAX220
- Orthosis, Spinal Pedicle FixationMNI197
- Spinal Vertebral Body Replacement DeviceMQP30
- Intervertebral Fusion Device With Bone Graft, CervicalODP17
- Screw, Fixation, BoneHWC15
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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