14 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
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
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
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·February 16, 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
R3 36MM ID US CRMC LINER 54
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDH·December 2, 2015
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·January 25, 2013
RESURFACING FEMORAL HEAD 50MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDI·February 28, 2018