ST. Jude Medical, Inc. Crmd
FDA adverse event reports naming ST. Jude Medical, Inc. Crmd as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ST. JUDE MEDICAL, INC. CRMD.
- Total reports
- 1,951
- Deaths
- 19
- Injuries
- 782
- Malfunctions
- 1,136
Reports per year
498
1899
3100
3101
2902
4103
3204
6005
17706
1,52814
Source: FDA adverse event reports by year received, 1998–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implantable Cardioverter Defibrillator (Non-Crt)LWS501
- Implantable Pacemaker Pulse-GeneratorDXY436
- Permanent Pacemaker ElectrodeDTB383
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK181
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN163
- Permanent Defibrillator ElectrodesNVY106
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP77
- Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)MXC51
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX30
- Sucker, Cardiotomy Return, Cardiopulmonary BypassDTS14
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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