Microport CRM S.r.l.
FDA adverse event reports naming Microport CRM S.r.l. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MICROPORT CRM S.R.L..
- Total reports
- 4,182
- Deaths
- 27
- Injuries
- 226
- Malfunctions
- 3,928
Reports per year
117
3719
20120
39621
37222
87423
1,04824
82225
43126
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP1,274
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN663
- Programmer, PacemakerKRG563
- Pacemaker/Icd/Crt Non-Implanted ComponentsOSR450
- Defibrillator, Implantable, Dual-ChamberMRM362
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK283
- Implantable Pacemaker Pulse-GeneratorDXY218
- Pulse Generator, Permanent, ImplantableNVZ154
- Implantable Cardioverter Defibrillator (Non-Crt)LWS146
- Permanent Pacemaker ElectrodeDTB46
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Microport CRM S.r.l. automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.