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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Hemashield Double Velour Cardiovascular Fabrics. Cardiovascular Devices Maquet Cardiovascular, LLC 2 United States USFDA
Device Recall Hemashield Platinum Woven and Knitted Double Velour Vascular Grafts. Cardiovascular Devices Maquet Cardiovascular, LLC 2 United States USFDA
Device Recall Hemashield Finesse Ultrathin Knitted Cardiovascular Patch. Cardiovascular Devices Maquet Cardiovascular, LLC 3 United States USFDA
Device Recall Hemashield Platinum Woven Double Velour TAAA Vascular Grafts. Cardiovascular Devices Maquet Cardiovascular, LLC 2 United States USFDA
Device Recall Hemashield Gold Woven and Knitted Double Vascular Grafts. Cardiovascular Devices Maquet Cardiovascular, LLC 2 United States USFDA
Device Recall Maximo II CRTD Cardiovascular Devices Medtronic Inc. Cardiac Rhythm Disease Managment 3 United States USFDA
Device Recall Maximo II DR Cardiovascular Devices Medtronic Inc. Cardiac Rhythm Disease Managment 3 United States USFDA
Device Recall Maximo II VR Cardiovascular Devices Medtronic Inc. Cardiac Rhythm Disease Managment 3 United States USFDA
Device Recall Secura DR Cardiovascular Devices Medtronic Inc. Cardiac Rhythm Disease Managment 3 United States USFDA
Device Recall Secura VR Cardiovascular Devices Medtronic Inc. Cardiac Rhythm Disease Managment 3 United States USFDA
Device Recall Medtronic Carelink Monitor Model 2490C Cardiovascular Devices Medtronic Inc. Cardiac Rhythm Disease Managment 3 United States USFDA
Device Recall Paradym Defibrillators Cardiovascular Devices ela Medical Llc 3 United States USFDA
Device Recall Virtuoso II DR Cardiovascular Devices Medtronic Inc. Cardiac Rhythm Disease Managment 3 United States USFDA
Device Recall Virtuoso II VR Cardiovascular Devices Medtronic Inc. Cardiac Rhythm Disease Managment 3 United States USFDA
Device Recall enpath Myopore Bipolar 54 cm Epicardial Lead Sutureless Myocardial Pacing Lead Cardiovascular Devices Greatbatch Medical 3 United States USFDA
Device Recall PeriStrips Dry Staple Line Reinforcement with Apex Processing (PSD) and PeriStrips Dry with Verita Cardiovascular Devices Synovis Surgical Inovation Div. of 2 United States USFDA
Device Recall Guidant, CONTAK RENEWAL 3/3RF Cardiovascular Devices Boston Scientific CRM Corp 3 United States USFDA
Device Recall Hemashield Finesse UltraThin Knitted Cardiovascular Patch Cardiovascular Devices Maquet Cardiovascular, LLC 2 United States USFDA
Device Recall SynerGraft CryoValve Cardiovascular Devices CryoLife, Inc. 3 United States USFDA
Device Recall LATITUDE Patient Management System Cardiovascular Devices Boston Scientific CRM Corp 3 United States USFDA
Device Recall SynerGraft CryoValve Pulmonary Valve and Conduit SG Cardiovascular Devices CryoLife, Inc. 2 United States USFDA
Device Recall SynerGraft CryoPatch Pulmonary HemiArtery SG Cardiovascular Devices CryoLife, Inc. 2 United States USFDA
Device Recall SJM Confirm, Implantable Cardiac Monitor (ICM) Cardiovascular Devices St Jude Medical CRMD 2 United States USFDA
Accent DR Cardiovascular Devices St Jude Medical CRMD 3 United States USFDA
LATITUDE Patient Management System Cardiovascular Devices Boston Scientific CRM Corp 3 United States USFDA