5 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
COBAS 8000 C 502 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·October 31, 2024
PUMP IN STYLE (ITEM # UNK)
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·February 14, 2014
ENDURANT II STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·October 23, 2012
ESPRIT VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC.·Product code CBK·August 16, 2010
PHOS2
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEO·October 1, 2024