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MicroVention Web Aneurysm Embolization
No active recall
Manufacturer: MicroVention · FDA product code: OPR · Category: Intrasaccular Flow Disruption Device
Severity Snapshot
37 total reports2019-10 – 2026-02 date range91.9% physician / facility reported8.1% manufacturer reported2 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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