MULClass 2
Generator, Electrosurgical, Coagulation, Cancer
FDA adverse event reports and recall history for generator, electrosurgical, coagulation, cancer (product code MUL), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 150
- Deaths
- 0
- Injuries
- 22
- Malfunctions
- 128
Reports per year
106
208
109
2012
7413
5014
115
126
Source: FDA adverse event reports by year received, 2006–2026. 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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