Back to Neurovascular
Stent
No active recall
FDA product code: NJE · Category: Intracranial Neurovascular Stent
Severity Snapshot
445 total reports1993-06 – 2026-03 date range37.5% physician / facility reported62.5% manufacturer reported3 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…