Cardiac Pacemakers, Inc
FDA adverse event reports naming Cardiac Pacemakers, Inc as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CARDIAC PACEMAKERS, INC.
- Total reports
- 34,149
- Deaths
- 542
- Injuries
- 13,486
- Malfunctions
- 20,121
Reports per year
199
1,04303
2,35904
2,43705
6,74706
9,82607
11,73308
111
112
123
Source: FDA adverse event reports by year received, 1999–2023. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Implantable Cardioverter Defibrillator (Non-Crt)LWS19,272
- Permanent Pacemaker ElectrodeDTB7,092
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK4,037
- Implantable Pacemaker Pulse-GeneratorDXY3,353
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP207
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)NKE114
- Pulse Generator, Permanent, ImplantableNVZ32
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN16
- Permanent Defibrillator ElectrodesNVY10
- Pacemaker Lead AdaptorDTD8
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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