26 results
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24ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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EUROMI
FDA Adverse Event
Malfunction
·EUROMI·Product code GEA·March 29, 2023
EUROMI REUSABLE CANNULA
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·June 27, 2023
CANNULA
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·April 17, 2023
CANULE VITERBO 3*250 MM TUNGSTÈNE
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·April 14, 2023
CANNULA
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·April 17, 2023
REBELO 5*350 TITANIUM
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·June 28, 2023
CANNULAS
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·November 8, 2024
EURO-MED
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code KNW·October 3, 2007
EURO-MED
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code KNW·July 12, 2007
EURO-MED
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code KNW·April 2, 2008
HL20 INTEGRATED PERFUSION SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·August 1, 2016
HL20 INTEGRATED PERFUSION SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·January 14, 2016
EURO-MED ROTATING HANDLE
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HFB·April 13, 2018
CENTRIFUGAL PUMP CONSOLE
FDA Adverse Event
Malfunction
·LIVANOVA DUTSCHLAND GMBH·Product code KFM·August 14, 2020
CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DWA·December 21, 2020
MAQUET HL-20 INTEGRATED PERFUSION SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·March 23, 2016
TWIN ROLLER PUMP INTEGRATED PERFUSION SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·October 12, 2016
HL20 INTEGRATED PERFUSION SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·October 21, 2015
SCP DRIVE UNIT W/FAST CLAMP
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND GMBH·Product code DWA·December 22, 2023
SYRINGE 30ML LL S/C 56
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·August 28, 2024