Stryker Spine-us
FDA adverse event reports naming Stryker Spine-us as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER SPINE-US.
- Total reports
- 2,405
- Deaths
- 2
- Injuries
- 1,147
- Malfunctions
- 1,256
Reports per year
1813
3514
12515
11716
5617
40518
30019
30620
30621
14522
10723
22724
15425
10426
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Thoracolumbosacral Pedicle Screw SystemNKB961
- Orthopedic Manual Surgical InstrumentLXH418
- Intervertebral Fusion Device With Bone Graft, LumbarMAX372
- Posterior Cervical Screw SystemNKG210
- Appliance, Fixation, Spinal Intervertebral BodyKWQ178
- Intervertebral Fusion Device With Integrated Fixation, CervicalOVE57
- Appliance, Fixation, Spinal InterlaminalKWP49
- Spinal Vertebral Body Replacement DeviceMQP29
- Intervertebral Fusion Device With Integrated Fixation, LumbarOVD25
- Intervertebral Fusion Device With Bone Graft, CervicalODP24
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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