DSRClass 3
Stimulator, Carotid Sinus Nerve
FDA adverse event reports and recall history for stimulator, carotid sinus nerve (product code DSR), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 416
- Deaths
- 31
- Injuries
- 381
- Malfunctions
- 4
Reports per year
115
116
317
118
119
521
2422
6023
9324
13725
9026
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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