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
- 5,087
- Deaths
- 72
- Injuries
- 2,000
- Malfunctions
- 3,000
Top device categories
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN1,505
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK1,112
- Leadless PacemakerPNJ720
- Permanent Defibrillator ElectrodesNVY538
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP460
- Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)MXC265
- Implantable Cardioverter Defibrillator (Non-Crt)LWS179
- Pulse Generator, Permanent, ImplantableNVZ178
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX41
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)NKE34
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Abbott Medical (crm-sylmar) automatically
DeviceWatch monitors available FDA adverse events and recalls. Growth includes event alerts for Death and Injury reports; Compliance Pro adds safety signals for investigation. FDA publication delays and incomplete collection or analysis coverage limit detection; no signal does not establish the absence of a safety concern. AI summaries and signals are provisional and require human review.