Stryker Endoscopy Puerto Rico
FDA adverse event reports naming Stryker Endoscopy Puerto Rico as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER ENDOSCOPY PUERTO RICO.
- Total reports
- 1,214
- Deaths
- 0
- Injuries
- 95
- Malfunctions
- 1,106
Reports per year
1004
5605
2906
6207
10408
21809
30110
23811
18812
813
Source: FDA adverse event reports by year received, 2004–2013. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI610
- ArthroscopeHRX263
- Apparatus, Suction, Operating-Room, Wall Vacuum PoweredGCX102
- Burr, OrthopedicHTT68
- Fastener, Fixation, Nondegradable, Soft TissueMBI42
- Drill, Surgical, Ent (Electric Or Pneumatic) Including HandpieceERL19
- Cutter, SurgicalFZT13
- Bit, DrillHTW9
- Anchor, Suture, Bone Fixation, MetallicNOV9
- Bur, Surgical, General & Plastic SurgeryGFF8
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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