FZEClass 2
Prosthesis, Nose, Internal
FDA adverse event reports and recall history for prosthesis, nose, internal (product code FZE), from the public MAUDE 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 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.
Monitor prosthesis, nose, internal automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.