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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller Cardiovascular Devices Thoratec Corporation 3 United States USFDA
Device Recall Zenith Alpha Thoracic Endovascular Graft Cardiovascular Devices Cook Medical Incorporated 3 United States USFDA
Device Recall BioGlue Cardiovascular Devices CryoLife, Inc. 3 United States USFDA
Device Recall bileaflet mechanical heart valve Cardiovascular Devices CryoLife, Inc. 3 United States USFDA
Device Recall OnX Ascending Aortic Prosthesis with the Vascutek Gelweave Valsalva Graft Cardiovascular Devices CryoLife, Inc. 3 United States USFDA
Device Recall EMBLEM SICD, Model A209, Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall EMBLEM MRI SICD Model 219 Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall SQRX 1010 Pulse Generator Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall MyCareLink Patient Monitor Cardiovascular Devices Medtronic Inc., Cardiac Rhythm and Heart Failure 3 United States USFDA
Device Recall MyCareLink Smart Patient Monitor Cardiovascular Devices Medtronic Inc., Cardiac Rhythm and Heart Failure 3 United States USFDA
Device Recall Platinium VR 1210 Cardiovascular Devices Sorin Group Italia SRL - CRF 3 United States USFDA
Device Recall Platinium DR 1510 Cardiovascular Devices Sorin Group Italia SRL - CRF 3 United States USFDA
Device Recall Platinium CRT DF1 1711 Cardiovascular Devices Sorin Group Italia SRL - CRF 3 United States USFDA
Device Recall Platinium VR DF4 1240 Cardiovascular Devices Sorin Group Italia SRL - CRF 3 United States USFDA
Device Recall Platinium DR DF4 1540 Cardiovascular Devices Sorin Group Italia SRL - CRF 3 United States USFDA
Device Recall Platinium CRTD 1741 Cardiovascular Devices Sorin Group Italia SRL - CRF 3 United States USFDA
Device Recall Fortify, Fortify Assura Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Unify and Unify Assura Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Anthem, Allure Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Assurity, Assurity Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Assurity MRI Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Merlin Patient Care System Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall MerlinHome Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Nuance Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Accent family of pacemakers Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA