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
- 3,969
- Deaths
- 15
- Injuries
- 3,431
- Malfunctions
- 512
Reports per year
109
10710
47611
1,12312
1,35413
90414
415
Source: FDA adverse event reports by year received, 2009–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW2,494
- Stimulator, Spinal-Cord, Implanted (Pain Relief)GZB1,434
- Stimulator, Peripheral Nerve, Implanted (Pain Relief)GZF36
- Implantable Cardioverter Defibrillator (Non-Crt)LWS2
- Stylet, Tracheal TubeBSR1
- Unit, PhacofragmentationHQC1
- Media, ReproductiveMQL1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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