Medtronic Singapore Operations
FDA adverse event reports naming Medtronic Singapore Operations as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: Medtronic Singapore Operations.
- Total reports
- 1,784
- Deaths
- 16
- Injuries
- 615
- Malfunctions
- 1,153
Top device categories
- Permanent Pacemaker ElectrodeDTB591
- Pulse Generator, Permanent, ImplantableNVZ542
- Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)MXD423
- Implantable Cardioverter Defibrillator (Non-Crt)LWS191
- Detector And Alarm, ArrhythmiaDSI21
- Permanent Defibrillator ElectrodesNVY10
- Implantable Pacemaker Pulse-GeneratorDXY3
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN2
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)NKE1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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