3 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 4, 2014
LIFEPAK CR(R) PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·December 21, 2012
NON-PVC RECEPT.LINER 200ML/CE(50/CS)
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code GCX·October 15, 2010