11 results
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41ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
RESOLUTE INTEGRITY RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·September 4, 2019
MAYFIELD TRIAD SKULL CLAMP
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·September 22, 2014
RESTORE ULTRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 12, 2015
RESOLUTE INTEGRITY RX
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·January 20, 2018
EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 30, 2023
EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 10, 2023
COGNIS
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 3, 2014
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·May 29, 2013
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 25, 2011
EDWARDS SAPIEN 3 ULTRA TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·March 6, 2024
EDWARDS SAPIEN 3 ULTRA RESILIA TRANSCATHETER HEART VALVE / P140031
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 6, 2024