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
- 4,116
- Deaths
- 23
- Injuries
- 224
- Malfunctions
- 3,868
Reports per year
117
3719
20120
39621
37222
87423
1,04824
82125
36626
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP1,260
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN643
- Programmer, PacemakerKRG549
- Pacemaker/Icd/Crt Non-Implanted ComponentsOSR448
- Defibrillator, Implantable, Dual-ChamberMRM355
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK278
- Implantable Pacemaker Pulse-GeneratorDXY214
- 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.
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