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
- 42,071
- Deaths
- 408
- Injuries
- 19,081
- Malfunctions
- 22,582
Reports per year
113
814
615
716
1217
3218
4819
5520
7621
11822
20623
37524
19,27825
21,84926
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 ElectrodeDTB22,493
- Implantable Cardioverter Defibrillator (Non-Crt)LWS7,847
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN5,761
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX2,684
- Permanent Defibrillator ElectrodesNVY2,393
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY288
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationOAE201
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP157
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW77
- Implantable Pacemaker Pulse-GeneratorDXY41
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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