NPSClass 3
Tricuspid Valve Repair Device, Percutaneously Delivered
FDA adverse event reports and recall history for tricuspid valve repair device, percutaneously delivered (product code NPS), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 2,028
- Deaths
- 77
- Injuries
- 1,234
- Malfunctions
- 717
Reports per year
122
54624
93125
55026
Source: FDA adverse event reports by year received, 2022–2026. 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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