GDHClass 1
Gouge, Surgical, General & Plastic Surgery
FDA adverse event reports and recall history for gouge, surgical, general & plastic surgery (product code GDH), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 156
- Deaths
- 0
- Injuries
- 14
- Malfunctions
- 138
Reports per year
211
212
213
714
1215
716
1317
318
419
220
521
222
223
224
226
Source: FDA adverse event reports by year received, 2011–2026. 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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