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Artis Zee Multi-Purpose
No active recall
FDA product code: OWB · Category: Interventional Fluoroscopic X-Ray System
Severity Snapshot
47 total reports2016-07 – 2024-05 date range25.5% physician / facility reported74.5% manufacturer reported2 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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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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