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Nombre Fecha Fecha de inicio País Fuente
Retiro De Equipo (Recall) de VALITUDE CRT-P 2017-12-20 Australia DHTGA
Retiro De Equipo (Recall) de Brio Charging System Model 6721 (used with Deep Brain Stimulator, Brio IPG Model 65-6788) 2015-09-15 Australia DHTGA
Retiro De Equipo (Recall) de Optisure Dual Coil Defibrillation Leads(Lead, defibrillator/pacemaker, implantable 2015-11-06 Australia DHTGA
Retiro De Equipo (Recall) de St. Jude Medical ICD/CRT-D devices programmed to a single VF detection zone with Merlin Programmer software version 17.2.2 rev. 0 Affected ICD/CRT-D devices: Current/Promote/AnalyST, Unify/Fortify, Assura and Ellipse families 2014-01-23 Australia DHTGA
Retiro De Equipo (Recall) de Eon Mini Implantable Pulse Generator (IPG) Model 65-3788 and Eon Mini Charging System Model 3721 2014-12-10 Australia DHTGA
Retiro De Equipo (Recall) de RF enabled St. Jude Medical Ellipse, Fortify Assura, Unify Assura, and Quadra Assura Implantable Cardioverter Defibrillators (ICDs) and Assurity and Allure Pacemakers when used with Merlin@home RF Remote Monitoring Transmitter Model EX1150 2015-08-20 Australia DHTGA
Retiro De Equipo (Recall) de Eon, Eon Mini and Brio Implantable Pulse Generator (IPG) (Implantable Spinal Cord and Deep Brain Stimulators) 2012-08-09 Australia DHTGA
Retiro De Equipo (Recall) de Eon Mini and Brio Implantable Pulse Generators (IPG) (Implantable Spinal Cord and Deep Brain Stimulators) 2012-08-03 Australia DHTGA
Retiro De Equipo (Recall) de Fortify, Fortify Assura, Quadra Assura, Unify, Unify Assura and Unify Quadra(Implantable cardiac defibrillator (ICD) and cardiac resynchronization therapy defibrillator (CRT-D) devices) 2016-10-11 Australia DHTGA
Retiro De Equipo (Recall) de AGA Medical Amplatzer Septal Occluder Amplatzer Septal Occluder, 28mm 2014-06-03 Australia DHTGA
Retiro De Equipo (Recall) de St. Jude Medical Ellipse VR/DR Implantable Cardioverter Defibrillators (ICDs) 2014-08-18 Australia DHTGA
Retiro De Equipo (Recall) de Eon/Eon C/ Eon Mini/ Prodigy Neurostimulation Systems and Octrode/ Quattrode Percutaneous Leads and Accessories 2014-12-10 Australia DHTGA
Retiro De Equipo (Recall) de RF enabled St. Jude Medical Ellipse, Fortify Assura, Unify Assura, and Quadra Assura Implantable Cardioverter Defibrillators (ICDs) and Assurity and Allure Pacemakers when used with Merlin@home RF Remote Monitoring Transmitter Model EX1150 2014-12-19 Australia DHTGA
Retiro De Equipo (Recall) de Eon Wall Charger Model 3701 and Eon Portable Charger 2015-05-29 Australia DHTGA
Retiro De Equipo (Recall) de SJM Confirm External Patient Activator Model DM2100ASupplied separately or together with a SJM Confirm Implantable Cardiac Monitor (ICM) DM2100 or DM2102 2013-04-15 Australia DHTGA
Alerta De Seguridad para Product Name: EON MINI NEUROSTIMULATION SYSTEM Technical Name: EON MINI NEUROSTIMULATION SYSTEM ANVISA Registration Number: 10332340246 Hazard Class: IV Hazard Class: 3788 2017-02-02 Brazil ANVISA
Alerta De Seguridad para The Field Action affects five products registered in Brazil. FORTIFY ™ - Registration 10332340305. UNIFY - Registration 10332340299. Fortify Assura VR - Registration 10332340358. Unify Assura - Registration 10332340344. Implantable Cardioverter and Defibrillator Quadra Assura - Record 10332340343 2016-10-24 Brazil ANVISA
Alerta De Seguridad para Business Name: HeartMate 3 - Left Ventricular Assist System. Technical Name: Other Cardiovascular Implants. ANVISA registration number: 10332340428. Class of risk: IV. Affected Model: HeartMate 3. Serial Numbers Affected: Model: 10010167 - Series Numbers: MLP-009201; MLP-009203; MLP-009205, MLP-009206; MLP-009207; MLP-009667 2018-04-17 Brazil ANVISA
Alerta De Seguridad para Implantable Defibrillator Software:. EPIC HF V-339. EPIC + V-196. EPIC + V-236. EPIC + HF V-350. ATLAS + V-193. ATLAS + V-243. ATLAS + HF V-341. ATLAS + II V-268 2008-01-28 Brazil ANVISA
Alerta De Seguridad para Implantable Defibrillator (Photon DR V-230), Registry 10332340083; Implantable Defibrillator (Photon DR V-232), Register 10332340090 Implantable Defibrillator (Photon VR V-194), Registry 10332340092, Implantable Cardioverter Defibrillator (Atlas DR V-240 V-199), Register 10332340093. 2005-10-25 Brazil ANVISA
Alerta De Seguridad para ACCORDING TO THE ANNEX List .... 2011-02-24 Brazil ANVISA
Retiro De Equipo (Recall) de 1500T14 CARDIAC ABLATION SYSTEM - GENERATOR 2011-05-09 Canada HC
Retiro De Equipo (Recall) de NANOSTIM LEADLESS PACEMAKER NANOSTIM DELIVERY SYSTEM CATHETER 2016-10-24 Canada HC
Retiro De Equipo (Recall) de FORTIFY ASSURA DR 2016-10-10 Canada HC
Retiro De Equipo (Recall) de PORT-A-CATH II DUAL LUMEN SYSTEM 2013-09-06 Canada HC