FDAClass 2
Enteroscope And Accessories
FDA adverse event reports and recall history for enteroscope and accessories (product code FDA), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 780
- Deaths
- 10
- Injuries
- 333
- Malfunctions
- 432
Reports per year
212
213
314
215
516
2817
8118
7619
2920
2421
8722
7223
8624
11925
15026
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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