DWGClass 2
Electrosurgical Device
FDA adverse event reports and recall history for electrosurgical device (product code DWG), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 254
- Deaths
- 1
- Injuries
- 42
- Malfunctions
- 209
Reports per year
392
103
106
510
1312
12213
8414
915
217
118
523
624
226
Source: FDA adverse event reports by year received, 1992–2026. 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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