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Terumo Radifocus Guide Wire
No active recall
Manufacturer: Terumo · FDA product code: DQX · Category: Wire, Guide, Catheter
Severity Snapshot
21 total reports1992-09 – 2025-07 date range22.2% physician / facility reported77.8% manufacturer reported4 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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