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Cordis Reflex Steerable Guidewire
No active recall
Manufacturer: Cordis · FDA product code: DQX · Category: Wire, Guide, Catheter
Severity Snapshot
26 total reports1998-07 – 2016-09 date range3.8% physician / facility reported96.2% manufacturer reported1 SKU variants
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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