Stryker Spine Bordeaux
FDA adverse event reports naming Stryker Spine Bordeaux as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER SPINE BORDEAUX.
- Total reports
- 2,578
- Deaths
- 1
- Injuries
- 664
- Malfunctions
- 1,901
Reports per year
304
7905
8706
6607
24608
52309
51910
43711
57612
4213
Source: FDA adverse event reports by year received, 2004–2013. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Thoracolumbosacral Pedicle Screw SystemNKB599
- Orthopedic Manual Surgical InstrumentLXH547
- Appliance, Fixation, Spinal Intervertebral BodyKWQ388
- Appliance, Fixation, Spinal InterlaminalKWP272
- ScrewdriverHXX113
- Intervertebral Fusion Device With Bone Graft, LumbarMAX99
- Orthosis, Spinal Pedicle FixationMNI97
- Screw, Fixation, BoneHWC78
- Orthosis, Spondylolisthesis Spinal FixationMNH74
- Intervertebral Fusion Device With Bone Graft, CervicalODP53
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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