KGEClass 2
Forceps, Biopsy, Electric
FDA adverse event reports and recall history for forceps, biopsy, electric (product code KGE), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 428
- Deaths
- 0
- Injuries
- 87
- Malfunctions
- 336
Reports per year
3012
1413
1214
1515
916
2617
2618
1519
720
2421
1622
823
924
1025
426
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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