5 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
OXIMAX N-595 PULSE OXIMETER
FDA Adverse Event
Malfunction
·COVIDIEN FORMERLY TYCO HEALTHCARE·Product code DQA·October 3, 2008
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·July 29, 2011
CUSA EXCEL 36KHZ STRAIGHT HANDPIECE
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES IRELAND LIMITED·Product code LFL·June 24, 2013
INSPIRE 7M HOLLOW FIBER OXYGENATOR, INSPIRE 7 DUAL HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·June 14, 2019
INSPIRE 7M HOLLOW FIBER OXYGENATOR, INSPIRE 7 DUAL HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·June 19, 2019