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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Lotus Valve System Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall Lotus Valve System Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall Lotus Valve System Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall Protg Rx Tapered Carotid Stent System Cardiovascular Devices Ev3, Inc. 3 United States USFDA
Device Recall Protg Rx Tapered Carotid Stent System Cardiovascular Devices Ev3, Inc. 3 United States USFDA
Device Recall Merlinhome RF Remote Monitoring Transmitter, Model EX1150, with software versions 6.1M or 7.0 Cardiovascular Devices St Jude Medical Cardiac Rhythm Management Division 3 United States USFDA
Device Recall HeartWare Ventricular Assist System Cardiovascular Devices HeartWare Inc 3 United States USFDA
Device Recall VASCUGUARD Pheripheral Vascular Patch Cardiovascular Devices Synovis Surgical Innovations, Inc. 2 United States USFDA
Device Recall Gelseal Cardiovascular Devices Vascutek, Ltd. 2 United States USFDA
Device Recall Gelseal Cardiovascular Devices Vascutek, Ltd. 2 United States USFDA
Device Recall Medtronic EnVeo R Loading System Cardiovascular Devices Medtronic Cardiovascular Surgery-the Heart Valve Division 3 United States USFDA
Device Recall WATCHMAN Left Atrial Appendage Closure Device with Delivery System Cardiovascular Devices Boston Scientific Corporation Not Classified United States USFDA
Device Recall WATCHMAN Access System Access Sheath with Dilator Cardiovascular Devices Boston Scientific Corporation Not Classified United States USFDA
Device Recall Optisure HV lead Cardiovascular Devices St Jude Medical Cardiac Rhythm Management Division 3 United States USFDA
Device Recall InSync III Cardiovascular Devices Medtronic Inc. 3 United States USFDA
Device Recall Bard Denali IVC Filter Cardiovascular Devices Bard Peripheral Vascular Inc 2 United States USFDA
Device Recall Zilver 518RX Vascular Stent Cardiovascular Devices Cook Medical Incorporated 3 United States USFDA
Device Recall Bard Distaflo Vascular Bypass Graft Cardiovascular Devices Bard Peripheral Vascular Inc 2 United States USFDA
Device Recall Bard Distaflo Vascular Bypass Graft Cardiovascular Devices Bard Peripheral Vascular Inc 2 United States USFDA
Device Recall MitraClip Clip Delivery System Cardiovascular Devices Abbott Vascular 3 United States USFDA
Device Recall Denali FilterJugular Subclavian Delivery System Cardiovascular Devices Bard Peripheral Vascular Inc 2 United States USFDA
Device Recall Denali Filter Femoral Delivery System Cardiovascular Devices Bard Peripheral Vascular Inc 2 United States USFDA
Device Recall Ventricular Assist Device Cardiovascular Devices HeartWare Inc 3 United States USFDA
Device Recall Carelink and Carelink Express Monitor Cardiovascular Devices Medtronic Inc., Cardiac Rhythm and Heart Failure 3 United States USFDA
Device Recall Ellipse Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA