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Galaxy G3 Mini
No active recall
FDA product code: KRD · Category: Device, Vascular, For Promoting Embolization
Severity Snapshot
466 total reports2018-07 – 2024-08 date range37.3% physician / facility reported62.7% manufacturer reported12 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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