KGWClass 2
Ring (Wound Protector), Drape Retention, Internal
FDA adverse event reports and recall history for ring (wound protector), drape retention, internal (product code KGW), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 183
- Deaths
- 0
- Injuries
- 16
- Malfunctions
- 167
Reports per year
111
1216
5817
1318
1119
1220
421
1822
1323
1924
1525
726
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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