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
- 34,145
- Deaths
- 542
- Injuries
- 13,486
- Malfunctions
- 20,117
Reports per year
199
1,04303
2,35804
2,43705
6,74506
9,82707
11,73308
123
Source: FDA adverse event reports by year received, 1999–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implantable Cardioverter Defibrillator (Non-Crt)LWS19,271
- Permanent Pacemaker ElectrodeDTB7,091
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK4,036
- Implantable Pacemaker Pulse-GeneratorDXY3,352
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP207
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)NKE114
- Pulse Generator, Permanent, ImplantableNVZ33
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN15
- Permanent Defibrillator ElectrodesNVY10
- Pacemaker Lead AdaptorDTD8
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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