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Name Date Date initiated Country Source
Recall of St Jude Medical Ellipse VR CD1377-36C Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2277-36 Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1377-36QC Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2377-36QC Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2377-36 Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1277-36 Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1377-36 Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2377-36Q Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1277-36Q Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1377-36Q Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2277-36Q Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2377-36C Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Merlin @ Home 2014-12-24 New Zealand NZMMDSA
Recall of VALITUDE X4 CRT-P U128 2017-12-15 New Zealand NZMMDSA
Recall of PROPONENT MRI SR Pacemaker L210 2017-12-15 New Zealand NZMMDSA
Recall of VISIONIST CRT-P U225 2017-12-15 New Zealand NZMMDSA
Recall of ACCOLADE MRI SR Pacemaker L310 2017-12-15 New Zealand NZMMDSA
Recall of Device Recall ACCOLADE MRI EL DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall Merlinhome RF Remote Monitoring Transmitter, Model EX1150, with software versions 6.1M or 7.0 2014-12-18 United States USFDA
Recall of Device Recall TactiSys Quartz Pack, PN004 400 2014-11-25 United States USFDA
Recall of Device Recall Optisure HV lead 2015-11-03 United States USFDA
Recall of Device Recall VALITUDE CRTP Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall VALITUDE X4 CRTP Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ALTRUA 2 SR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ALTRUA 2 DR Pacemaker 2017-12-07 United States USFDA