MEDTRONIC MOSAIC HEART VALVE Adverse Events: FDA MAUDE Data

MEDTRONIC, INC. · Replacement Heart Valve (Surgical/Transcatheter)

Total Reports

101

Reports (30d)

65

Active Signals

0

Open Recalls

0

Monthly Report Volume
Event Type Breakdown

Most commonly reported problems

1

Post-Implant Intervention for Unknown Reason

medtronic received, effects, received information, post implant, aortic bioprosthetic

23

reports

2

Evaluation for Transcatheter Replacement After Years

evaluated transcatheter, patient evaluated, reason evaluation, evaluation reported, replacement reason

22

reports

3

Permanent Pacemaker for Post-Implant Arrhythmias

pacemaker, implanted reason, permanent, post implant, permanent pacemaker

9

reports

Problem groupings are generated by Claripulse from report narrative text. They summarize what reporters wrote, not adjudicated root cause.

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Disclaimer: This system analyzes publicly available FDA MAUDE data. It does NOT provide medical advice. MAUDE data is de-identified. Do not attempt re-identification. Report counts may differ from the FDA's MAUDE search due to processing cadence and deduplication. Data is updated weekly.