Guidant CRM Clonmel Ireland
FDA adverse event reports naming Guidant CRM Clonmel Ireland as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: GUIDANT CRM CLONMEL IRELAND.
- Total reports
- 79,198
- Deaths
- 851
- Injuries
- 43,613
- Malfunctions
- 34,706
Reports per year
904
3305
9706
14907
28908
9,17009
8,70110
7,76211
4,92812
5,56713
7,47614
6,85415
8,91416
9,20317
10,04518
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 Cardioverter Defibrillator (Non-Crt)LWS29,666
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP28,113
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK12,872
- Pulse Generator, Permanent, ImplantableNVZ4,385
- Implantable Pacemaker Pulse-GeneratorDXY2,163
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)NKE1,136
- Programmer, PacemakerKRG587
- Permanent Pacemaker ElectrodeDTB222
- Permanent Defibrillator ElectrodesNVY18
- Pacemaker/Icd/Crt Non-Implanted ComponentsOSR14
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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