Guidant Puerto Rico Bv
FDA adverse event reports naming Guidant Puerto Rico Bv as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: GUIDANT PUERTO RICO BV.
- Total reports
- 2,240
- Deaths
- 56
- Injuries
- 1,067
- Malfunctions
- 1,114
Reports per year
302
52609
29410
31411
21812
14113
17414
17415
17016
14317
8118
223
Source: FDA adverse event reports by year received, 2002–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implantable Cardioverter Defibrillator (Non-Crt)LWS770
- Permanent Pacemaker ElectrodeDTB398
- Permanent Defibrillator ElectrodesNVY237
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN200
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP167
- Pulse Generator, Permanent, ImplantableNVZ119
- Implantable Pacemaker Pulse-GeneratorDXY82
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK78
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX46
- Wire, Guide, CatheterDQX29
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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