4 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code LDD·April 30, 2014
INSIGNIA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·October 10, 2012
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 26, 2007
G7 DUAL MOBILITY LINER 44MM F
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LPH·July 14, 2021