7 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
FIRSTPASS MINI LEFT
FDA Adverse Event
Malfunction
·ARTHROCARE CORP.·Product code NBH·December 12, 2019
MARKERS
FDA Adverse Event
Malfunction
·PRAXIM·Product code HAW·January 3, 2007
NAVLOCK
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code KCT·October 15, 2025
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·April 2, 2013
QUADRA ASSURA CRT-D
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·August 22, 2014
ENDURANT ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·March 18, 2011
4.2MM THREE-FLUTED DRILL BIT QC/330MM/100MM CALIBRATION
FDA Adverse Event
Injury
·SYNTHES USA·Product code HTW·October 14, 2016