24 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
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
ADVANTA V12,COVERED STENT SYS,9X59X80
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code NIO·April 7, 2026
STARDRIVE SCREWDRIVER SHAFT T4/66MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·May 20, 2014
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
UNKNOWN·Product code ITJ·November 5, 2012
ON-Q PAINBUSTER
FDA Adverse Event
Other
·I-FLOW CORP.·Product code MEB·August 25, 2010
ADVANTA V12 COVERED STENT SYSTEM
FDA Adverse Event
Injury
·ATRIUM MEDICAL CORPORATION·Product code NIO·August 13, 2025