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
- 57,916
- Deaths
- 854
- Injuries
- 21,144
- Malfunctions
- 35,918
Reports per year
5612
27113
53714
69115
1,10416
1,66417
2,63418
3,53419
3,43520
4,89321
6,23622
8,50923
9,57424
9,82225
4,95126
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Permanent Pacemaker ElectrodeDTB24,977
- Pulse Generator, Permanent, ImplantableNVZ13,957
- Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)MXD9,727
- Implantable Cardioverter Defibrillator (Non-Crt)LWS6,190
- Detector And Alarm, ArrhythmiaDSI1,911
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN519
- Permanent Defibrillator ElectrodesNVY399
- Implantable Pacemaker Pulse-GeneratorDXY169
- 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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