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  • Device 27
  • Manufacturer 92
  • Event 253
  • Implant 4
Name Date Date initiated Country Source
Recall Or Safety Alert for Implantable pulse generators Brio ™ 2012-04-17 Spain AEMPSVFOI
Recall Or Safety Alert for "NanostimTM Wireless Pacemaker & Placement System Catheter", model S1DLCP 2014-08-04 Spain AEMPSVFOI
Recall Or Safety Alert for "Portico ™ Transcatheter Transcatheter Transcatheter Valve Transfemoral Implantation System" 2014-10-08 Spain AEMPSVFOI
Recall Or Safety Alert for "NanostimTM Wireless Pacemaker & Placement System Catheter", model S1DLCP 2015-03-03 Spain AEMPSVFOI
Recall Or Safety Alert for "Portico ™ transcatheter transcatheter transcatheter aortic valve implantation system", models PRT-23 and PRT-25 2015-03-24 Spain AEMPSVFOI
Recall Or Safety Alert for "NanostimTM Wireless Pacemaker & Placement System Catheter", model S1DLCP 2015-07-16 Spain AEMPSVFOI
Recall Or Safety Alert for Defibrillators (ICDs) and implantable pacemakers with radiofrequency (RF) capability 2015-08-19 Spain AEMPSVFOI
Recall Or Safety Alert for Fortified ™ Implantable Cardioverter Defibrillators, FortifyAssura ™, QuadraAssura ™, QuadraAssura MP ™, Unify ™, UnifyAssura ™ and UnifyQuadra ™ 2016-10-19 Spain AEMPSVFOI
Recall Or Safety Alert for NanostimTM wireless cardiac pacemaker, model S1DLCP 2016-11-02 Spain AEMPSVFOI
Recall Or Safety Alert for NanostimTM wireless cardiac pacemaker, model S1DLCP and "Nanostim Programmer Link" 2017-02-16 Spain AEMPSVFOI
Recall Or Safety Alert for Merlin @ Home ™ Model EX2000 Software for the Merlin @ Home ™ Transmitter, EX1150, EX1150W, EX1100, and EX1100W 2017-04-12 Spain AEMPSVFOI
Recall Or Safety Alert for Implantable Automatic Defibrillators (DAIs) EllipseTM VR / DR, models CD1411-36Q, CD1411-36C, CD2411-36Q, CD2411-36C, CD1377-36QC, CD1377-36C, CD2377-36QC and CD2377-36C 2016-04-12 Spain AEMPSVFOI
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
translation missing: en.activerecord.attributes.event.titles.recall_field_safety_notice 2015-11-10 Saudi Arabia SFDA
translation missing: en.activerecord.attributes.event.titles.recall_field_safety_notice 2017-10-12 Saudi Arabia SFDA
translation missing: en.activerecord.attributes.event.titles.recall_field_safety_notice 2011-05-28 Saudi Arabia SFDA
translation missing: en.activerecord.attributes.event.titles.recall_field_safety_notice 2017-11-19 Saudi Arabia SFDA
translation missing: en.activerecord.attributes.event.titles.recall_field_safety_notice 2012-04-03 Saudi Arabia SFDA
Field Safety Notices about Merlin@HomeTM Software for Merlin@HomeTM Transmitter (EX1150, EX1150W, EX1100, and EX1100W) 2017-04-03 Netherlands IGJ
Field Safety Notices about Nanostim™ Leadless Pacemaker 2017-05-11 Netherlands IGJ
Field Safety Notices about Nanostim™ Leadless Pacemaker 2017-11-17 Netherlands IGJ
Field Safety Notices about CardioMems Hospital and Patient Electronic System 2018-06-14 Netherlands IGJ
Field Safety Notices about AMPLATZER™ Septal Occluder 2014-01-02 Germany BAM
Field Safety Notices about Epic, Atlas and Convert 2008-01-18 Germany BAM
Field Safety Notices about Livewire TC 2008-06-26 Germany BAM
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About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

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.