3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
M2A-MAGNUM PF CUP 58ODX52ID
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·April 11, 2013
TERUMO ADVANCED PERFUSION SYSTEM 1
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·March 1, 2011
PLUM XLMD PUMP
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·May 21, 2008