1,359 results · 68ms · Sources: EU EUDAMED, US FDA

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PROTEK DUO VENO-VENOUS CANNULA

FDA Adverse Event
Malfunction ·LIVANOVA USA INC.·Product code DWF·March 18, 2026

TANDEMHEART PUMP

FDA Adverse Event
Malfunction ·CARDIACASSIST INC.·Product code KFM·December 23, 2020

TANDEMLUNG OXYGENATOR

FDA Adverse Event
Injury ·CARDIACASSIST INC.·Product code DTZ·May 13, 2020

TANDEMLUNG OXYGENATOR

FDA Adverse Event
Injury ·CARDIACASSIST INC.·Product code DTZ·January 12, 2022

PROTEK DUO VENO-VENOUS CANNULA

FDA Adverse Event
Injury ·CARDIACASSIST INC.·Product code DWF·May 7, 2021

TANDEMLUNG OXYGENATOR

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTZ·October 15, 2020

TANDEHEART PUMP

FDA Adverse Event
Injury ·CARDIAC ASSIST, INC.·Product code KFM·May 23, 2014

TANDEMHEART PUMP

FDA Adverse Event
Malfunction ·CARDIAC ASSIST, INC.·Product code KFM·April 10, 2014

TANDEMHEART

FDA Adverse Event
Injury ·CARDIAC ASSIST, INC·Product code DSQ·August 1, 2003

TANDEMHEART PUMP

FDA Adverse Event
Malfunction ·CARDIAC ASSIST, INC.·Product code KFM·June 11, 2007

TANDEMHEART ESCORT CONTROLLER

FDA Adverse Event
Malfunction ·CARDIAC ASSIST, INC.·Product code KFM·February 8, 2013

TANDEMHEART

FDA Adverse Event
Death ·CARDIAC ASSIST, INC·Product code KFM·October 1, 2010

TANDEMHEART TRANSSEPTAL CANNULA - EF

FDA Adverse Event
Injury ·CARDIAC ASSIST, INC.·Product code DWF·February 17, 2014

TANDEMHEART SYSTEM

FDA Adverse Event
Death ·CARDIAC ASSIST INC.·Product code KFM·June 18, 2009

TANDEMHEART SYSTEM

FDA Adverse Event
Injury ·CARDIAC ASSIST, INC.·Product code KFM·December 17, 2010

TANDEM HEART PERCUTANEOUS PTVA PUMP

FDA Adverse Event
Malfunction ·CARDIAC ASSIST, INC.·Product code DSQ·February 8, 2007

TANDEMHEART PUMP

FDA Adverse Event
Malfunction ·CARDIAC ASSIST, INC.·Product code KFM·March 1, 2007

TANDEMHEART

FDA Adverse Event
Death ·CARDIAC ASSIST, INC.·Product code DSQ·March 28, 2006

TANDEMHEART PUMP

FDA Adverse Event
Malfunction ·CARDIAC ASSIST, INC.·Product code KFM·March 23, 2006

TANDEMHEART PUMP

FDA Adverse Event
Malfunction ·CARDIAC ASSIST, INC.·Product code KFM·December 2, 2005