23 results · 31ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEM CORP·Product code GEI·March 13, 2014

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 13, 2012

LIFEVEST WCD 3100 SYSTEM

FDA Adverse Event
Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·September 3, 2010

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

NAVITOR TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Death ·ABBOTT MEDICAL·Product code NPT·December 2, 2025

NAVITOR TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code NPT·December 2, 2025

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

ALINITY M HR HPV AMP KIT

FDA Adverse Event
Malfunction ·ABBOTT MOLECULAR, INC.·Product code MAQ·February 26, 2024

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

NAVITOR TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Malfunction ·ABBOTT MEDICAL·Product code NPT·May 28, 2026

NAVITOR TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code NPT·May 28, 2026