HANCOCK Adverse Events: FDA MAUDE Data
MEDTRONIC, INC. · Replacement Heart Valve (Surgical/Transcatheter) · First cleared Sep 1989
Total Reports
313
Reports (30d)
0
Active Signals
0
Open Recalls
0
What the reports describe · Claripulse analysis
Most commonly reported problems
Evaluation for Transcatheter Replacement Post-Implant
mosaic aortic, medtronic received, reported medtronic, intervention, mosaic
4
reports
Evaluation for Valve Replacement Post-Implant
evaluated transcatheter, reason evaluation, patient evaluated, evaluation reported, replacement reason
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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