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Name Date Date initiated Country Source
Recall of SYNCHROMED II - PROGRAMMABLE PUMP 2017-04-27 Canada HC
Recall of SYNCHROMED II - PROGRAMMABLE PUMP 2011-02-22 Canada HC
Recall of SYNCHROMED II - PROGRAMMABLE PUMP 2014-03-05 Canada HC
Recall of RESTOREADVANCED MULTI-PROGRAM NEUROSTIMULATOR - N'VISION APPLICATION CARD 2017-03-09 Canada HC
Recall of N'VISION APPLICATION CARD 2012-03-14 Canada HC
Recall of SYNCHROMED II - PROGRAMMABLE PUMP 2011-09-05 Canada HC
Recall of SYNCHROMED II - PROGRAMMABLE PUMP 2008-06-18 Canada HC
Recall of N'VISION APPLICATION CARD 2013-10-26 Canada HC
Recall of SYNCHROMED II - PROGRAMMABLE PUMP 2017-08-22 Canada HC
Recall of SYNCHROMED II - PROGRAMMABLE PUMP 2011-11-25 Canada HC
Field Safety Notices about SynchroMed® II Implantable Drug Pumps 2014-03-27 Ireland HPRA
Field Safety Notices about SynchroMed® II and SynchroMed EL Implantable Drug Pumps 2013-07-11 Ireland HPRA
Field Safety Notices about SynchroMed® II Implanteerbare Infusiepomp 2017-04-14 Netherlands IGJ
Field Safety Notices about SynchroMed® II Implanteerbare Infusiepomp 2017-11-15 Netherlands IGJ
Recall of Synchromed II 2008-06-06 France ANSM
Recall of Synchromed II 2016-03-16 France ANSM
Recall of Synchromed II 2015-04-23 France ANSM
Safety Alert Or Field Safety Notices for SynchroMed® implantable drug pump 2003-10-22 United Kingdom MHRA
Safety Alert Or Field Safety Notices for SynchroMed EL models 8626 and 8627 and SynchroMed II model 8637 implantable drug pumps 2008-12-18 United Kingdom MHRA
Safety Alert Or Field Safety Notices for Implantable drug pumps and accessories 2013-06-19 United Kingdom MHRA
Recall of Medtronic SynchroMed II Infusion Pump 2012-11-07 New Zealand NZMMDSA
Recall of SynchroMed® II pump 2017-05-05 New Zealand NZMMDSA
Recall of Medtronic - 8840 N'Vision 2017-01-24 New Zealand NZMMDSA
Field Safety Notices about implantable synchromed infusion pumps. 2011-01-24 Poland ORMPMDBP
Field Safety Notices about implanted infusion pumps synchromed ii 2016-11-14 Poland ORMPMDBP