Abbott Medical (crm-sylmar)
FDA adverse event reports naming Abbott Medical (crm-sylmar) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: Abbott Medical (CRM-Sylmar).
- Total reports
- 2,767
- Deaths
- 47
- Injuries
- 1,095
- Malfunctions
- 1,615
Top device categories
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN825
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK600
- Leadless PacemakerPNJ392
- Permanent Defibrillator ElectrodesNVY300
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP251
- Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)MXC132
- Implantable Cardioverter Defibrillator (Non-Crt)LWS102
- Pulse Generator, Permanent, ImplantableNVZ93
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)NKE21
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX21
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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