GCMClass 2
Endoscope, Rigid
FDA adverse event reports and recall history for endoscope, rigid (product code GCM), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 1,495
- Deaths
- 1
- Injuries
- 11
- Malfunctions
- 1,482
Reports per year
197
209
114
115
616
317
118
519
120
521
422
223
44924
61625
39226
Source: FDA adverse event reports by year received, 1997–2026. 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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