FGCClass 2
Urethroscope
FDA adverse event reports and recall history for urethroscope (product code FGC), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 1,762
- Deaths
- 0
- Injuries
- 7
- Malfunctions
- 1,755
Reports per year
195
100
115
117
221
3322
34623
45524
56025
36226
Source: FDA adverse event reports by year received, 1995–2026. 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.
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