EWYClass 2
Mediastinoscope, Surgical
FDA adverse event reports and recall history for mediastinoscope, surgical (product code EWY), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 364
- Deaths
- 0
- Injuries
- 23
- Malfunctions
- 340
Reports per year
200
206
110
111
215
1216
217
421
922
9723
9924
10525
2826
Source: FDA adverse event reports by year received, 2000–2026. 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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