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Protege RX Carotid Stent
No active recall
FDA product code: NIM · Category: Stent, Carotid
Severity Snapshot
408 total reports2009-04 – 2026-03 date range33.6% physician / facility reported66.4% 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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