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
- 7,244
- Deaths
- 27
- Injuries
- 2,910
- Malfunctions
- 4,302
Reports per year
Source: FDA adverse event reports by year received, 2008–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Permanent Pacemaker ElectrodeDTB3,818
- Implantable Cardioverter Defibrillator (Non-Crt)LWS1,202
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN1,048
- Permanent Defibrillator ElectrodesNVY561
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX475
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY43
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP27
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW19
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationOAE18
- Implantable Pacemaker Pulse-GeneratorDXY11
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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