1,854 results
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64ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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MEDTRONIC PERIPHERAL (FORMERLY COVIDIEN VASCULAR / EV3)
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NIO·September 13, 2022
SURGIPRO II
FDA Adverse Event
Malfunction
·DAVIS & GECK CARIBE LTD·Product code GAW·May 10, 2024
VALIANT STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·October 22, 2019
ENDURANT II STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·October 22, 2019
EVOLUT FX DCS
FDA Adverse Event
Malfunction
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 1, 2025
LAPRO-CLIP
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GCJ·August 2, 2022
ATTAIN SELECT II + SUREVALVE
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code DQY·October 28, 2016
ZINGER GUIDEWIRE
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code DQX·December 16, 2016
ASSURANT BALLOON EXPANDABLE STENT SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code DQY·September 14, 2015
LAUNCHER 6F (EBU3.5)
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code DQY·March 30, 2009
INPUT PS
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code DYB·February 4, 2010
MEDTRONIC COMPLETE SE BILIARY
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code FGE·April 21, 2010
MEDTRONIC CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code NIE·March 19, 2012
COUGAR
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code DQX·December 8, 2014
RESOLUTE INTEGRITY RX DES
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code NIQ·September 2, 2015
GUARDWIRE PLUS 200CM J
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code NFA·September 15, 2003
GUARDWIRE PLUS 200CM J
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code NFA·September 15, 2003
RELIANT STENT GRAFT BALLOON CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code DQY·April 12, 2007
ANEURX AAADVANTAGE STENT GRAFT SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code MIH·May 29, 2007
GUARDWIRE PLUS OCCLUSION DEVICE-JAPAN
FDA Adverse Event
Malfunction
·MEDTRONIC VASCULAR·Product code NFA·April 3, 2007