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Guidant 4
No active recall
FDA product code: DXC · Category: Clamp, Vascular
Severity Snapshot
3,367 total reports2003-01 – 2008-10 date range0% physician / facility reported100% manufacturer reported43 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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