ST. Jude Medical - Neuromodulation
FDA adverse event reports naming ST. Jude Medical - Neuromodulation as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ST. JUDE MEDICAL - NEUROMODULATION.
- Total reports
- 94,255
- Deaths
- 293
- Injuries
- 85,211
- Malfunctions
- 8,588
Reports per year
28310
4,18811
9,69312
13,71013
7,85814
7,31315
6,40616
8,49517
13,12518
13,60219
9,58220
Source: FDA adverse event reports by year received, 2010–2020. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW53,589
- Stimulator, Spinal-Cord, Implanted (Pain Relief)GZB30,903
- Dorsal Root Ganglion Stimulator For Pain ReliefPMP6,121
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY1,918
- Stimulator, Peripheral Nerve, Implanted (Pain Relief)GZF1,640
- Cover, Burr HoleGXR17
- Implantable Cardioverter Defibrillator (Non-Crt)LWS15
- Catheter, CholangiographyGBZ8
- Product code ------6
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)NIK5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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