Guidant Clonmel Ireland
FDA adverse event reports naming Guidant Clonmel Ireland as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: GUIDANT CLONMEL IRELAND.
- Total reports
- 1,215
- Deaths
- 75
- Injuries
- 438
- Malfunctions
- 702
Reports per year
204
405
1306
707
3708
51809
28210
17711
5312
4313
3014
1415
1716
1317
418
Source: FDA adverse event reports by year received, 2004–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implantable Pacemaker Pulse-GeneratorDXY462
- Pulse Generator, Permanent, ImplantableNVZ356
- Implantable Cardioverter Defibrillator (Non-Crt)LWS308
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP82
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK6
- 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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