9 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNIFY QUADRA CRT-D, DF4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·May 2, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 15, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 11, 2011
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC·Product code HAW·July 25, 2023
ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY
FDA Adverse Event
Injury
·COOK INC·Product code MIH·June 30, 2017
ZENITH FLEX WITH SPIRAL-Z TECHNOLOGY AAA ENDOVASCULAR GRAFT ILIAC LEG
FDA Adverse Event
Injury
·COOK INC·Product code MIH·June 30, 2017
TRU CC FEMORAL SIZE 4 LEFT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 6, 2024
UNKNOWN PATELLA COMPONENT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 6, 2024
ZENITH AAA ENDOVASCULAR GRAFT ILIAC LEG
FDA Adverse Event
Injury
·COOK INC·Product code MIH·November 27, 2019