Back to Neuronavigation
Artis Zeego
No active recall
FDA product code: OWB · Category: Interventional Fluoroscopic X-Ray System
Severity Snapshot
90 total reports2012-06 – 2025-08 date range21.1% physician / facility reported78.9% manufacturer reported1 SKU variants
Failure & Consequence Profiles
Top Failure Modes
Click any bar to view those reports ↓
Top Patient Outcomes
Click any bar to view those reports ↓
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.
Filter by failure mode
Filter by outcome
Loading reports…