HANCOCK Adverse Events: FDA MAUDE Data
MEDTRONIC, INC. · Replacement Heart Valve (Surgical/Transcatheter) · First cleared Mar 2009 · 14 device variants grouped
Total Reports
344
Reports (30d)
3
Active Signals
0
Open Recalls
0
What the reports describe · Claripulse analysis
Most commonly reported problems
Post-Implant Evaluation for Valve Replacement
reason evaluation, adverse, medtronic received, effects, post implant
6
reports
Evaluation for Transcatheter Replacement Post-Implant
patient evaluated, evaluation reported, replacement reason, reported years, evaluated transcatheter
1
reports
Permanent Pacemaker for Complete Heart Block
pacemaker, pacemaker implanted, implanted reason, permanent, permanent pacemaker
1
reports
Problem groupings are generated by Claripulse from report narrative text. They summarize what reporters wrote, not adjudicated root cause.
Evidence
Related research
Citations indexed from PubMed.
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