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No active recall
Manufacturer: Boston Scientific · FDA product code: KRD · Category: Device, Vascular, For Promoting Embolization
Severity Snapshot
405 total reports2011-08 – 2025-12 date range0% physician / facility reported0% 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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