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Echotip Ultra Fiducial Needle
No active recall
FDA product code: NEU · Category: Marker, Radiographic, Implantable
Severity Snapshot
58 total reports2012-11 – 2022-08 date range3.4% physician / facility reported96.6% 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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