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Cordis Aquatrack
No active recall
Manufacturer: Cordis · FDA product code: DQX · Category: Wire, Guide, Catheter
Severity Snapshot
11 total reports2012-05 – 2026-02 date range88.9% physician / facility reported11.1% manufacturer reported3 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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