FZEClass 2
Prosthesis, Nose, Internal
FDA adverse event reports and recall history for prosthesis, nose, internal (product code FZE), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 211
- Deaths
- 0
- Injuries
- 206
- Malfunctions
- 2
Reports per year
198
100
204
208
716
1317
1218
2419
2320
3221
3022
1423
2624
1325
426
Source: FDA adverse event reports by year received, 1998–2026. 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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