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
- 12,660
- Deaths
- 8
- Injuries
- 1,283
- Malfunctions
- 11,369
Reports per year
61913
1,06714
1,15515
1,25316
1,26017
75018
59119
56220
74721
82322
1,34023
1,01124
1,04625
43626
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Laparoscope, General & Plastic SurgeryGCJ2,017
- Endoscopic Grasping/Cutting Instrument, Non-PoweredOCZ1,986
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI1,948
- Product code KOGKOG1,055
- ArthroscopeHRX788
- Fastener, Fixation, Nondegradable, Soft TissueMBI735
- Confocal Optical ImagingOWN655
- Blade, Saw, General & Plastic Surgery, SurgicalGFA582
- Apparatus, Suction, Operating-Room, Wall Vacuum PoweredGCX433
- Accessories, ArthroscopicNBH415
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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