FDCClass 2
Resectoscope, Working Element
FDA adverse event reports and recall history for resectoscope, working element (product code FDC), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 440
- Deaths
- 2
- Injuries
- 91
- Malfunctions
- 303
Reports per year
2712
2113
2914
1215
116
917
418
1419
1020
521
522
923
1124
2125
1926
Source: FDA adverse event reports by year received, 2012–2026. 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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