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/AEMS corpus and the live FDA recall database.
- Total reports
- 1,943
- Deaths
- 74
- Injuries
- 1,182
- Malfunctions
- 687
Reports per year
122
54624
93125
46526
Source: FDA adverse event reports by year received, 2022–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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