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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
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
Device Recall AFX Endovascular AAA System, Endoleak Type IIIA Cardiovascular Devices Endologix 3 United States USFDA
Device Recall AFX Endovascular AAA System Cardiovascular Devices Endologix 3 United States USFDA
Device Recall AFX Endovascular AAA System Cardiovascular Devices Endologix 3 United States USFDA
Device Recall AFX Endovascular AAA System, Endoleak Type IIIB Cardiovascular Devices Endologix 3 United States USFDA
Device Recall AFX Endovascular AAA System Cardiovascular Devices Endologix 3 United States USFDA
Device Recall AFX Endovascular AAA System Cardiovascular Devices Endologix 3 United States USFDA
Device Recall AFX Endovascular AAA System Cardiovascular Devices Endologix 3 United States USFDA
Device Recall AFX2 Endovascular AAA System Cardiovascular Devices Endologix 3 United States USFDA
Device Recall SICD Programmer Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall HeartWare Ventricular Assist System Cardiovascular Devices Heartware 3 United States USFDA
Device Recall Endurant / Endurant II 23mm and 25mm Bifurcated Stent Graft Systems Cardiovascular Devices Medtronic Vascular, Inc. 3 United States USFDA
Device Recall Cordis S.M.A.R.T. Flex Vascular Stent System Cardiovascular Devices Cordis Corporation 3 United States USFDA
Device Recall Heartware Ventricular Assist System Cardiovascular Devices Heartware 3 United States USFDA
Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller Cardiovascular Devices Thoratec Corporation 3 United States USFDA
Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller Cardiovascular Devices Thoratec Corporation 3 United States USFDA