HFGClass 2
Coagulator, Laparoscopic, Unipolar (And Accessories)
FDA adverse event reports and recall history for coagulator, laparoscopic, unipolar (and accessories) (product code HFG), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 254
- Deaths
- 5
- Injuries
- 162
- Malfunctions
- 79
Reports per year
209
210
314
215
516
217
318
519
620
2021
2022
3623
2124
3225
2126
Source: FDA adverse event reports by year received, 2009–2026. 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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