NPUClass 3
Prosthesis, Mitral Valve, Percutaneously Delivered
FDA adverse event reports and recall history for prosthesis, mitral valve, percutaneously delivered (product code NPU), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 1,930
- Deaths
- 415
- Injuries
- 1,377
- Malfunctions
- 138
Reports per year
1117
5118
3019
21820
24821
21322
28823
28024
31525
27626
Source: FDA adverse event reports by year received, 2017–2026. 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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