Medtronic Puerto Rico Villalba
FDA adverse event reports naming Medtronic Puerto Rico Villalba as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: Medtronic Puerto Rico Villalba.
- Total reports
- 4,052
- Deaths
- 14
- Injuries
- 1,689
- Malfunctions
- 2,345
Reports per year
113
114
416
117
418
719
420
1721
322
223
624
525
3,99726
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Permanent Pacemaker ElectrodeDTB2,106
- Implantable Cardioverter Defibrillator (Non-Crt)LWS722
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN562
- Permanent Defibrillator ElectrodesNVY305
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX267
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY30
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP16
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW12
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationOAE12
- Implantable Pacemaker Pulse-GeneratorDXY7
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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