Vista de la lista Vista de las tarjetas
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Zenex Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Assurity Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Allure Quadra Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Everflex SelfExpanding Peripheral Stent with Entrust Delivery System Cardiovascular Devices Medtronic Inc. 3 United States USFDA
Device Recall Innova SelfExpanding Stent System Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall Certitude Delivery System Cardiovascular Devices Edwards Lifesciences, LLC 3 United States USFDA
Device Recall ACCOLADE SR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ACCOLADE DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ACCOLADE EL DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ACCOLADE MRI SR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ACCOLADE MRI DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ACCOLADE MRI EL DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall VALITUDE CRTP Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall VALITUDE X4 CRTP Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ALTRUA 2 SR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ALTRUA 2 DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ALTRUA 2 EL DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall VISIONIST CRTP Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall VISIONIST X4 CRTP Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ESSENTIO SR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ESSENTIO DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ESSENTIO MRI SR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ESSENTIO MRI DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ESSENTIO EL DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA
Device Recall ESSENTIO MRI EL DR Pacemaker Cardiovascular Devices Boston Scientific Corporation 3 United States USFDA