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 during the 2026 MAUDE-to-AEMS transition 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.
Monitor Stryker Spine Bordeaux automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.