3,989 results
·
57ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
OUTBACK ELITE RE-ENTRY CATHETER
FDA Adverse Event
Malfunction
·CORDIS US CORP.·Product code PDU·May 11, 2022
TEMPO
FDA Adverse Event
Malfunction
·CORDIS US CORP·Product code DQO·September 24, 2024
SABER
FDA Adverse Event
Malfunction
·CORDIS US. CORP·Product code LIT·August 22, 2024
POWERFLEX EXTREME
FDA Adverse Event
Malfunction
·CORDIS US. CORP·Product code LIT·July 23, 2024
TEMPO
FDA Adverse Event
Malfunction
·CORDIS US CORP·Product code DQO·September 24, 2024
OUTBACK
FDA Adverse Event
Malfunction
·CORDIS US. CORP·Product code PDU·July 7, 2024
SABER
FDA Adverse Event
Malfunction
·CORDIS US. CORP·Product code LIT·September 19, 2024
OPTEASE
FDA Adverse Event
Malfunction
·CORDIS US CORP·Product code DTK·September 24, 2024
TEMPO
FDA Adverse Event
Malfunction
·CORDIS US CORP·Product code DQO·September 24, 2024
TEMPO
FDA Adverse Event
Malfunction
·CORDIS US CORP·Product code DQO·July 3, 2024
VISTA BRITE TIP
FDA Adverse Event
Malfunction
·CORDIS US CORP.·Product code DQY·July 10, 2024
MYNX CONTROL VENOUS
FDA Adverse Event
Malfunction
·CORDIS US CORP·Product code MGB·September 30, 2024
AVANTI
FDA Adverse Event
Malfunction
·CORDIS US CORP.·Product code DRE·September 26, 2024
POWERFLEX PRO
FDA Adverse Event
Malfunction
·CORDIS US. CORP·Product code LIT·July 1, 2024
SABERX RADIANZ
FDA Adverse Event
Malfunction
·CORDIS US. CORP·Product code LIT·September 4, 2024
TEMPO
FDA Adverse Event
Malfunction
·CORDIS US CORP·Product code DQO·July 2, 2024
POWERFLEX PRO
FDA Adverse Event
Malfunction
·CORDIS US. CORP·Product code LIT·August 23, 2024
TEMPO
FDA Adverse Event
Malfunction
·CORDIS US. CORP·Product code DQO·September 23, 2024
CATHETER EXTENSION
FDA Adverse Event
Malfunction
·CORDIS US CORP·Product code DQO·September 3, 2024
SABERX RADIANZ
FDA Adverse Event
Malfunction
·CORDIS US. CORP·Product code LIT·September 30, 2024