4 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SURESCAN
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·June 9, 2020
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·March 1, 2013
MBT CEM KEEL TIB TRAY SZ5
FDA Adverse Event
Injury
·DEPUY (IRELAND)·Product code NJL·February 24, 2011
LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·March 12, 2008