ST. Jude Medical - Neuromodulation (puerto Rico, Llc)
FDA adverse event reports naming ST. Jude Medical - Neuromodulation (puerto Rico, Llc) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC).
- Total reports
- 62,638
- Deaths
- 131
- Injuries
- 61,156
- Malfunctions
- 1,350
Reports per year
1614
32415
66016
1,94117
3,42418
4,94419
6,08920
6,51721
7,16822
8,46923
9,83624
9,14425
4,10626
Source: FDA adverse event reports by year received, 2014–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW58,385
- Stimulator, Spinal-Cord, Implanted (Pain Relief)GZB3,816
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY236
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK46
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN31
- Permanent Defibrillator ElectrodesNVY31
- Dorsal Root Ganglion Stimulator For Pain ReliefPMP19
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP18
- Implantable Cardioverter Defibrillator (Non-Crt)LWS17
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX17
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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