Covidien LP (valleylab)
FDA adverse event reports naming Covidien LP (valleylab) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN LP (VALLEYLAB).
- Total reports
- 3,350
- Deaths
- 19
- Injuries
- 349
- Malfunctions
- 2,977
Reports per year
2907
41608
53009
78310
87811
70712
113
614
Source: FDA adverse event reports by year received, 2007–2014. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI3,183
- Electrosurgical Patient Return ElectrodeODR81
- System, Ablation, Microwave And AccessoriesNEY44
- Generator, Lesion, RadiofrequencyGXD11
- Instrument, Ultrasonic SurgicalLFL8
- Electrode, ElectrosurgicalJOS7
- Electrosurgical DeviceDWG5
- Unit, Electrosurgical And Coagulation, With AccessoriesBWA3
- Laparoscope, General & Plastic SurgeryGCJ3
- Generator, Shock-Wave, For Pain ReliefNBN2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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