567 results · 28ms · Sources: EU EUDAMED, US FDA

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MYCARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·May 3, 2018

MYCARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·May 3, 2018

MYCARELINK

FDA Adverse Event
Malfunction ·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·June 15, 2018

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·June 9, 2016

ADAPTA DR

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

ADAPTA D

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2015

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·March 27, 2015

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code NVZ·May 1, 2018

MEDTRONIC LEAD

FDA Adverse Event
Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

REVEAL XT

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DSI·August 9, 2016

ENRHYTHM

FDA Adverse Event
Death ·MEDTRONIC, INC.·Product code NVZ·December 23, 2014

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code NVZ·December 22, 2016

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·February 16, 2016

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Death ·MEDTRONIC, INC.·Product code DXY·February 23, 2016

VIRTUOSO DR

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code LWS·February 10, 2015

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2016

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval
FDA Class 3 ·SYNERGYST II PULSE GENERATOR MODELS 7070 & 7071

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval
FDA Class 3 ·CapSure VDD 2 Lead; Vitatron Brilliant S+ vdd Lead