4 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·April 6, 2011
LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 MEDIUM-LARGE TITANIUM LIGA
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code FZP·July 17, 2008
INTIMA-II Y 24GAX0.75IN PRN/EC SLM
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·November 6, 2025
INTIMA II
FDA Adverse Event
Malfunction
·BD SUZHOU (MDS)·Product code FOZ·April 3, 2026