4 results
·
14ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
INFUSION DEVICES - UNKNOWN
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 9, 2024
INFUSION DEVICES - UNKNOWN
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 9, 2024
OMEGA?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·June 19, 2014
LIFEPAK EXPRESS(R) DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·December 21, 2012