9 results
·
65ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
COVIDIEN LIGASURE
FDA Adverse Event
Injury
·MEDTRONIC/ FORMERLY COVIDIEN·Product code GEI·October 26, 2017
KANGAROO
FDA Adverse Event
Malfunction
·MEDTRONIC (FORMERLY COVIDIEN)·Product code KNT·May 10, 2016
MEDTRONIC PERIPHERAL (FORMERLY COVIDIEN VASCULAR / EV3)
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NIO·September 13, 2022
TI-CRON 2-0 STR W/10" SWGD NDL BX OF12
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code GAT·April 10, 2025
MEDTRONIC PERIPHERAL (FORMERLY COVIDIEN VASCULAR EV3) GUIDEWIRE
FDA Adverse Event
Injury
·MEDTRONIC/COVIDIEN LP·Product code DQX·August 28, 2025
UNKNOWN MICRO CATHETERS
FDA Adverse Event
Injury
·IRVINE·Product code KRA·June 12, 2015
ONYX AVM
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code MFE·June 12, 2015
PURITAN BENNETT BB980 VENTILATOR SYSTEM
FDA Adverse Event
Malfunction
·COVIDIEN / MEDTRONIC, FORMERLY NELLCOR PURITAN BENNETT, INC.·Product code CBK·November 28, 2018
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Malfunction
·MEDTRONIC/COVIDIEN FORMERLY MICRO THERAPEUTICS, INC. DBA EV·Product code OUT·November 14, 2016