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Faradrive
No active recall
FDA product code: DRA · Category: Catheter, Steerable
Severity Snapshot
754 total reports2024-05 – 2026-03 date range98.3% physician / facility reported1.7% manufacturer reported3 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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