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Perclose Proglide
No active recall
FDA product code: MGB · Category: Device, Hemostasis, Vascular
Severity Snapshot
3,088 total reports2022-01 – 2026-03 date range96.4% physician / facility reported3.6% manufacturer reported1 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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