Cardiva VASCADE 6/7F VCS Adverse Events: FDA MAUDE Data
CARDIVA MEDICAL, INC. · Vascular Hemostasis/Closure Device · First cleared Jan 2013
Total Reports
105
Reports (30d)
3
Active Signals
1
Open Recalls
0
What the reports describe · Claripulse analysis
Most commonly reported problems
Component Absence During Deployment Attempt
terumo medical, medical corporation, angio, received following, angio seal
2
reports
Problem groupings are generated by Claripulse from report narrative text. They summarize what reporters wrote, not adjudicated root cause.
Detection
Active safety signals
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