Stryker Trauma Kiel
FDA adverse event reports naming Stryker Trauma Kiel as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER TRAUMA KIEL.
- Total reports
- 7,824
- Deaths
- 70
- Injuries
- 5,315
- Malfunctions
- 2,439
Reports per year
108
109
27213
70914
50615
63316
38717
1,49518
98319
1,08620
83321
59322
13523
124
225
Source: FDA adverse event reports by year received, 2008–2025. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Rod, Fixation, Intramedullary And AccessoriesHSB5,142
- Orthopedic Manual Surgical InstrumentLXH1,434
- Screw, Fixation, BoneHWC672
- Nail, Fixation, BoneJDS161
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE106
- Pin, Fixation, SmoothHTY76
- Appliance, Fixation, Nail/Blade/Plate Combination, Multiple ComponentKTT44
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic FinishMAY28
- Plate, Fixation, BoneHRS22
- ScrewdriverHXX20
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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