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
- 12,572
- Deaths
- 8
- Injuries
- 1,269
- Malfunctions
- 11,295
Reports per year
61913
1,06714
1,15515
1,25316
1,26017
75018
59119
56220
74721
82322
1,34023
1,01124
1,04325
35126
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Laparoscope, General & Plastic SurgeryGCJ1,997
- Endoscopic Grasping/Cutting Instrument, Non-PoweredOCZ1,986
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI1,939
- Product code KOGKOG1,055
- ArthroscopeHRX772
- Fastener, Fixation, Nondegradable, Soft TissueMBI730
- Confocal Optical ImagingOWN647
- Blade, Saw, General & Plastic Surgery, SurgicalGFA569
- Apparatus, Suction, Operating-Room, Wall Vacuum PoweredGCX431
- Accessories, ArthroscopicNBH413
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Stryker Endoscopy-san Jose 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.