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  • Device 27
  • Manufacturer 92
  • Event 253
  • Implant 4
Name Date Date initiated Country Source
Safety Alert for Photon DR (Model V-230HV), Photon Micro VR/DR (Models V-194/V-232), Atlas VR/DR (Models V-199/V-240) 2005-10-10 Hong Kong DH
Safety Alert for 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
Field Safety Notices about St. Jude Medical ICD Photon 2005-11-24 Germany BAM
Safety Alert for APS III Model 3500/3510 programming devices (software versions 6.1.1 and earlier) and Merlin PCS Model 3650 programming devices (software versions 4.1.1 and earlier) 2006-10-19 Hong Kong DH
Field Safety Notices about Identity family of pacemakers 2006-10-20 Germany BAM
Field Safety Notices about Cardiac Positioning System CPS Direct SL, slittable CRT lead delivery tools 2007-08-10 Germany BAM
Field Safety Notices about Epic, Atlas and Convert 2008-01-18 Germany BAM
Safety Alert for 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
Field Safety Notices about Livewire TC 2008-06-26 Germany BAM
Field Safety Notices about EP-4 Computerised Cardiac Stimulator 2009-04-20 Germany BAM
Field Safety Notices about Epicor UltraWand LP Handheld Ablation device 2009-12-04 Germany BAM
Safety Alert for Convert+ Model V-195 Implantable Cardioverter-Defibrillator (ICD) 2010-05-06 Hong Kong DH
Field Safety Notices about implantable cardioverter defibrillators Convert+ V-195 2010-05-27 Germany BAM
Field Safety Notices about 6 Fr. Engage™ Introducers 2010-08-20 Germany BAM
Field Safety Notices about Riata and Riata ST silicone insulated defibrillation leads 2011-01-04 Germany BAM
Safety Alert for ACCORDING TO THE ANNEX List .... 2011-02-24 Brazil ANVISA
Field Safety Notices about Cardio Life Research MitraXs Self Adjusting Atrial Retractor 2011-03-03 Germany BAM
Field Safety Notices about Implantable Cardiac Monitors (Models CONFIRM DM2100 and DM2102) 2011-03-29 Germany BAM
Field Safety Notices about implantable pulse generators for neurostimulation EON MINI and BRIO 2011-05-31 Germany BAM
Field Safety Notices about the Accent DR dual-chamber pacemaker and the Anthem CRT-P 2011-09-26 Germany BAM
Field Safety Notices about Riata and Riata ST Silicone Endocardial Defibrillation leads 2011-12-15 Germany BAM
Recall Or Safety Alert for Implantable pulse generators: "Eon", Model 65-3716 and "Eon Mini", Model 65-3788 for stimulation of the spinal cord and "Brio", Model 65-6788 for deep brain stimulation, manufactured by St. Jude Medical USA 2012-01-05 Spain AEMPSVFOI
Field Safety Notices about implantable pulse generators for neurostimulation Eon Mini and Brio 2012-02-23 Germany BAM
Field Safety Notices about implantable pulse generators for neurostimulation Eon, Eon Mini and Brio 2012-02-24 Germany BAM
Safety Alert for QuickSite® and QuickFlex® Left Ventricular CRT Leads [Models 1056T, 1058T, 1156T and 1158T] 2012-04-12 Hong Kong DH
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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.