ONYX TRUCOR Adverse Events: FDA MAUDE Data

MEDTRONIC, INC. · Coronary Drug-Eluting Stent

Total Reports

175

Reports (30d)

8

Active Signals

2

Open Recalls

0

Monthly Report Volume
Event Type Breakdown

Most commonly reported problems

1

In-Vivo Dislodgement During Delivery

onyx frontier, coronary drug, onyx, inspected, frontier

29

reports

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

Active safety signals

Disproportionate reportinghighIncreasing trendmedium

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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.