Stryker Instruments-kalamazoo
FDA adverse event reports naming Stryker Instruments-kalamazoo as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER INSTRUMENTS-KALAMAZOO.
- Total reports
- 29,459
- Deaths
- 7
- Injuries
- 658
- Malfunctions
- 28,794
Reports per year
3,30113
4,63814
4,73815
2,83216
2,39417
2,82518
4,06719
3,39520
81821
14322
28623
1824
425
Source: FDA adverse event reports by year received, 2013–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Drill, Surgical, Ent (Electric Or Pneumatic) Including HandpieceERL10,174
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE5,007
- Drills, Burrs, Trephines & Accessories (Simple, Powered)HBE2,891
- Neurological Stereotaxic InstrumentHAW1,670
- ArthroscopeHRX1,588
- Driver, Wire, And Bone Drill, ManualDZJ1,361
- Unit, Operative DentalEIA1,094
- Motor, Drill, PneumaticHBB880
- Blade, Saw, General & Plastic Surgery, SurgicalGFA600
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI566
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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