Covidien MFG DC Boulder
FDA adverse event reports naming Covidien MFG DC Boulder as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN MFG DC BOULDER.
- Total reports
- 14,148
- Deaths
- 82
- Injuries
- 1,549
- Malfunctions
- 12,517
Reports per year
1,39017
1,68418
1,68419
1,55320
1,69721
1,57822
1,60323
2,27424
68525
Source: FDA adverse event reports by year received, 2017–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI12,218
- Instrument, Ultrasonic SurgicalLFL1,558
- Counter, Sponge, SurgicalLWH156
- System, Ablation, Microwave And AccessoriesNEY60
- Gauze/Sponge, Internal, X-Ray DetectableGDY39
- Unit, Electrosurgical And Coagulation, With AccessoriesBWA23
- Electrocautery, Gynecologic (And Accessories)HGI20
- Transmitters And Receivers, Physiological Signal, RadiofrequencyDRG19
- Apparatus, Exhaust, SurgicalFYD17
- Laparoscope, General & Plastic SurgeryGCJ9
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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