Back to Neurovascular
Xact Carotid Stent
No active recall
FDA product code: NIM · Category: Stent, Carotid
Severity Snapshot
1,281 total reports2006-02 – 2024-09 date range3.7% physician / facility reported96.3% manufacturer reported1 SKU variants
Reporting Trend
Annual Reporting Volume
Click any bar to view those reports ↓
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.
Loading reports…