6 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code GEI·December 12, 2014
HEARTMATE II SYSTEM CONTROLLER
FDA Adverse Event
Malfunction
·THORATEC CORP.·Product code DSQ·May 7, 2013
MAXI SKY
FDA Adverse Event
Malfunction
·BHM MEDICAL, INC.·Product code FSA·August 14, 2008
TRI-STAPLE 2.0
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·February 13, 2024
LIBRE 2 SENSOR FREESTYLE
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC·Product code QLG·February 9, 2024
LUMINOS AGILE
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code JAA·November 6, 2024