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Arrow International Fogarty
No active recall
Manufacturer: Arrow International · FDA product code: DXE · Category: Catheter, Embolectomy
Severity Snapshot
156 total reports1992-07 – 2026-03 date range63.4% physician / facility reported36.6% manufacturer reported5 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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