Kenstone Metal
FDA adverse event reports naming Kenstone Metal as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: KENSTONE METAL.
- Total reports
- 1,251
- Deaths
- 0
- Injuries
- 5
- Malfunctions
- 153
Reports per year
3111
21212
45113
48314
7415
Source: FDA adverse event reports by year received, 2011–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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