Stryker Endoscopy SAN Jose
FDA adverse event reports naming Stryker Endoscopy SAN Jose as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER ENDOSCOPY SAN JOSE.
- Total reports
- 3,267
- Deaths
- 0
- Injuries
- 248
- Malfunctions
- 2,988
Reports per year
2504
7605
6706
9507
9008
41109
96610
98111
51612
3913
115
Source: FDA adverse event reports by year received, 2004–2015. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Light Source, Fiberoptic, RoutineFCW1,469
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI384
- Light Source, Endoscope, Xenon ArcGCT309
- ArthroscopeHRX272
- Product code KOGKOG151
- Laparoscope, General & Plastic SurgeryGCJ111
- Camera, Television, Surgical, Without AudioFWB61
- Insufflator, LaparoscopicHIF61
- Accessories, ArthroscopicNBH42
- Insufflator, Automatic Carbon-Dioxide For EndoscopeFCX36
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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