ST. Jude Medical - Spinal Modulation
FDA adverse event reports naming ST. Jude Medical - Spinal Modulation as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ST. JUDE MEDICAL - SPINAL MODULATION.
- Total reports
- 1,628
- Deaths
- 3
- Injuries
- 1,615
- Malfunctions
- 10
Reports per year
28616
1,12917
21318
Source: FDA adverse event reports by year received, 2016–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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