Mpri
FDA adverse event reports naming Mpri as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MPRI.
- Total reports
- 293,075
- Deaths
- 5,422
- Injuries
- 165,438
- Malfunctions
- 122,214
Reports per year
16211
1,17012
16,02613
15,57814
15,98115
16,32916
15,61917
21,27418
24,58419
25,46720
25,74521
26,75822
36,49023
34,81924
16,94925
Source: FDA adverse event reports by year received, 2011–2025. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Permanent Pacemaker ElectrodeDTB154,673
- Implantable Cardioverter Defibrillator (Non-Crt)LWS67,378
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN28,483
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX23,181
- Permanent Defibrillator ElectrodesNVY10,401
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP4,874
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY1,295
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW833
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationOAE609
- Stimulator, Electrical, Implantable, For IncontinenceEZW483
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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