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Terumo Angioseal
No active recall
Manufacturer: Terumo · FDA product code: MGB · Category: Device, Hemostasis, Vascular
Severity Snapshot
161 total reports1998-02 – 2025-09 date range90.9% physician / facility reported9.1% manufacturer reported18 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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