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
- 58,545
- Deaths
- 859
- Injuries
- 21,361
- Malfunctions
- 36,325
Reports per year
5612
27113
53714
69115
1,10416
1,66417
2,63318
3,53419
3,43520
4,89321
6,23622
8,50923
9,57424
9,82225
5,58126
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Permanent Pacemaker ElectrodeDTB25,188
- Pulse Generator, Permanent, ImplantableNVZ14,142
- Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)MXD9,885
- Implantable Cardioverter Defibrillator (Non-Crt)LWS6,249
- Detector And Alarm, ArrhythmiaDSI1,918
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN521
- Permanent Defibrillator ElectrodesNVY405
- Implantable Pacemaker Pulse-GeneratorDXY170
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX61
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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