21 results · 29ms · Sources: EU EUDAMED, US FDA

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CAPSUREFIX

FDA Adverse Event
Malfunction ·MPRI·Product code DTB·June 10, 2014

CURLIN ADMINNISTRATION SET

FDA Adverse Event
Malfunction ·MOOG MED DEVICES GROUP·Product code FRN·October 31, 2012

COAGUCHEK ® XS SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·June 22, 2015

SYNCHROMED II

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 24, 2019

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

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 29, 2016