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/AEMS corpus and the live FDA recall database.
- Total reports
- 1,890
- Deaths
- 409
- Injuries
- 1,344
- Malfunctions
- 137
Reports per year
1117
5118
3019
21820
24821
21322
28823
28024
31525
23626
Source: FDA adverse event reports by year received, 2017–2026. 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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