Core-vent Bio-engineering
FDA adverse event reports naming Core-vent Bio-engineering as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CORE-VENT BIO-ENGINEERING.
- Total reports
- 3,107
- Deaths
- 1
- Injuries
- 3,074
- Malfunctions
- 3
Reports per year
1493
35794
92195
1,17096
64597
Source: FDA adverse event reports by year received, 1993–1997. 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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