3 results
·
14ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
URIC ACID REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code KNK·April 15, 2011
AUTOPULSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·January 31, 2013
MAXGUARD BLOOD COLLECTION DEVICE
FDA Adverse Event
Malfunction
·CAREFUSION CORP·Product code FMH·June 27, 2014