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
- 11,966
- Deaths
- 7
- Injuries
- 566
- Malfunctions
- 11,372
Reports per year
1604
4905
4706
3707
8908
1,17309
2,12110
4,47311
3,82212
13913
Source: FDA adverse event reports by year received, 2004–2013. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Drill, Surgical, Ent (Electric Or Pneumatic) Including HandpieceERL2,766
- Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/AttachmentKIJ2,289
- Drills, Burrs, Trephines & Accessories (Simple, Powered)HBE2,025
- Driver, Wire, And Bone Drill, ManualDZJ1,769
- Motor, Drill, PneumaticHBB655
- ArthroscopeHRX516
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE340
- Apparatus, Exhaust, SurgicalFYD288
- Motor, Surgical Instrument, Pneumatic PoweredGET245
- Pump, Infusion, ElastomericMEB218
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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