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
- 1,585
- Deaths
- 2
- Injuries
- 1,554
- Malfunctions
- 20
Reports per year
125
1,58426
Source: FDA adverse event reports by year received, 2025–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor St. Jude Medical - Neuromodulation (puerto Rico, Llc) 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.