Vista de la lista Vista de las tarjetas
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
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
Device Recall HVAD Cardiovascular Devices HeartWare Inc 3 United States USFDA
Device Recall Cordis PRECIS (R) PRO Rx Nitinol Stent System Cardiovascular Devices Cordis Corporation 3 United States USFDA
Device Recall Cordis PRECIS (R) Rx Nitinol Stent System Cardiovascular Devices Cordis Corporation 3 United States USFDA
Device Recall EV3 EverFiex" Selfexpanding Peripheral Stent System Cardiovascular Devices Ev3, Inc. 3 United States USFDA
Device Recall Medtronic, MyCareLink Patient Monitor Cardiovascular Devices Medtronic Inc., Cardiac Rhythm and Heart Failure 3 United States USFDA
Device Recall Synovis VASCUGUARD Peripheral Vascular Patch Cardiovascular Devices Baxter Healthcare Corp. 2 United States USFDA
Device Recall Accolade MRI and Essentio MRI pacemakers Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall Boston Scientific, INGEVITY MRI Leads, Sterile EO, RxOnly. Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall AdaptivCRT (aCRT) Cardiovascular Devices Medtronic Inc., Cardiac Rhythm and Heart Failure 3 United States USFDA
Device Recall ChordX Chordal Sizer Cardiovascular Devices On-X Life Technologies, Inc. 2 United States USFDA