CPI Plant - ST. Paul
FDA adverse event reports naming CPI Plant - ST. Paul as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CPI PLANT - ST. PAUL.
- Total reports
- 2,224
- Deaths
- 28
- Injuries
- 1,512
- Malfunctions
- 684
Reports per year
404
305
106
107
208
6909
3710
3411
1512
5313
11914
17515
41916
69517
59418
Source: FDA adverse event reports by year received, 2004–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP1,070
- Implantable Cardioverter Defibrillator (Non-Crt)LWS673
- Permanent Defibrillator ElectrodesNVY167
- Permanent Pacemaker ElectrodeDTB165
- Implantable Pacemaker Pulse-GeneratorDXY53
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN36
- Pulse Generator, Permanent, ImplantableNVZ23
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK14
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX14
- Programmer, PacemakerKRG6
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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