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
- 39,768
- Deaths
- 391
- Injuries
- 17,995
- Malfunctions
- 21,382
Reports per year
113
814
615
816
1417
3318
5119
6420
9421
13622
22923
40124
19,27625
19,44726
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Permanent Pacemaker ElectrodeDTB21,330
- Implantable Cardioverter Defibrillator (Non-Crt)LWS7,417
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN5,420
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX2,533
- Permanent Defibrillator ElectrodesNVY2,205
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY279
- Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationOAE194
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP151
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW75
- Implantable Pacemaker Pulse-GeneratorDXY42
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Medtronic Puerto Rico Villalba automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.