Stryker Osteosynthesis Kiel
FDA adverse event reports naming Stryker Osteosynthesis Kiel as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER OSTEOSYNTHESIS KIEL.
- Total reports
- 2,521
- Deaths
- 3
- Injuries
- 756
- Malfunctions
- 1,729
Reports per year
6007
27908
42009
57510
60711
55512
2513
Source: FDA adverse event reports by year received, 2007–2013. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Orthopedic Manual Surgical InstrumentLXH1,002
- Rod, Fixation, Intramedullary And AccessoriesHSB858
- Nail, Fixation, BoneJDS207
- ScrewdriverHXX122
- Screw, Fixation, BoneHWC101
- Bit, DrillHTW74
- ReamerHTO57
- Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/AttachmentHSZ16
- Wire, SurgicalLRN15
- Pin, Fixation, SmoothHTY11
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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