IPG MFG Switzerland
FDA adverse event reports naming IPG MFG Switzerland as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: IPG MFG SWITZERLAND.
- Total reports
- 18,340
- Deaths
- 361
- Injuries
- 10,167
- Malfunctions
- 7,812
Reports per year
209
210
4911
42712
2,96713
3,15714
3,22415
7,49116
69817
31518
819
Source: FDA adverse event reports by year received, 2009–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Detector And Alarm, ArrhythmiaDSI5,027
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK3,329
- Pulse Generator, Permanent, ImplantableNVZ3,084
- Implantable Cardioverter Defibrillator (Non-Crt)LWS2,778
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP1,982
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY737
- Implantable Pacemaker Pulse-GeneratorDXY621
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW480
- Stimulator, Electrical, Implantable, For IncontinenceEZW166
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)NKE54
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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