3 results
·
12ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code LDD·May 20, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·November 6, 2012
CENTRA BED
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·August 26, 2010