3 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·November 14, 2014
COMPACT EXCHANGE DEVICE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - LARGO·Product code KDJ·September 16, 2011
BLACKMAX-NEURO
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBB·July 29, 2013