Stryker Instruments-a Division OF Stryker Corp
FDA adverse event reports naming Stryker Instruments-a Division OF Stryker Corp as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP.
- Total reports
- 13,618
- Deaths
- 5
- Injuries
- 368
- Malfunctions
- 13,245
Reports per year
1919
18720
2,64421
2,43322
2,84423
2,45324
2,29125
74726
Source: FDA adverse event reports by year received, 2019–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Drill, Surgical, Ent (Electric Or Pneumatic) Including HandpieceERL4,747
- Drills, Burrs, Trephines & Accessories (Simple, Powered)HBE2,599
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE2,308
- Blade, Saw, General & Plastic Surgery, SurgicalGFA825
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI393
- Image Processing Device For Estimation Of External Blood LossPBZ268
- Motor, Drill, PneumaticHBB249
- Instrument, Ultrasonic SurgicalLFL246
- Unit, Operative DentalEIA226
- Neurological Stereotaxic InstrumentHAW226
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Stryker Instruments-a Division OF Stryker Corp 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.