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Angiodynamics Mini Stick Max
No active recall
Manufacturer: AngioDynamics · FDA product code: DRE · Category: Dilator, Vessel, For Percutaneous Catheterization
Severity Snapshot
21 total reports2016-01 – 2025-12 date range7.1% physician / facility reported92.9% manufacturer reported4 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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