26 results · 24ms · Sources: EU EUDAMED, US FDA

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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