Back to Cranial Surgery
Terumo Angio-Seal Vip
No active recall
Manufacturer: Terumo · FDA product code: MGB · Category: Device, Hemostasis, Vascular
Severity Snapshot
2,780 total reports2006-04 – 2025-03 date range34.3% physician / facility reported65.7% manufacturer reported11 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…