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/AEMS 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 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.
Monitor ring (wound protector), drape retention, internal automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.