111 results
·
33ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CLOSED APHERESIS KIT, PL732, 600 ML TRANSFER PACK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code GKT·May 6, 1998
AMICUS SEPARATOR SYSTEM
FDA Adverse Event
Injury
·FENWAL, INC.·Product code GKT·April 4, 2014
1L PL2410 PLASTIC STORAGE CONTAINER - 1000 ML
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code KSR·April 20, 2010
IL PL2410 PLASTIC STORAGE CONTAINER - 1000 ML
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code KSR·April 20, 2010
1L PL2410 PLASTIC STORAGE CONTAINER - 1000 ML
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code KSR·April 20, 2010
CLOSED SYSTEM APHERESIS KIT W/ RESTRICTOR TUBING
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code GKT·June 20, 2007
CLOSED SYSTEM KIT W/RESTRICTOR TUBING
FDA Adverse Event
Malfunction
·FENWAL, INC·Product code GKT·June 20, 2007
AMICUS SEPARATOR SYSTEM
FDA Adverse Event
Injury
·FENWAL INC.·Product code GKT·November 16, 2010
AMICUS SEPARATOR SYSTEM
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code GKT·October 16, 2009
PLASMALINK TRANSFER PACK
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code GKT·October 23, 2009
PLASMACELL-C DISPOSABLE KIT W/ ATTACHED FISTULA
FDA Adverse Event
Death
·FENWAL, INC.·Product code GKT·October 29, 2009
AMICUS SEPARATOR SYSTEM
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code GKT·October 16, 2009
LEUKOCONNECT PRE-STORAGE-RS-2000 TRANSFER PACK
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code CAK·June 5, 2009
*
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code KSR·July 9, 2014
FENWAL TRANSFER PACK CONTAINER 300ML
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code KSR·July 22, 2021
AMICUS SEPARATOR SYSTEM
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code LKN·July 29, 2014
*
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code FPA·October 26, 2012
PLASMACELL-C DISPOSABLE SET
FDA Adverse Event
Injury
·FENWAL, INC.·Product code GKT·August 1, 2007
CELL SEPARATOR APHERESIS KIT W/RESTRICTOR TUB
FDA Adverse Event
Malfunction
·FENWAL, INC.·Product code GKT·August 3, 2007
FENWAL
FDA Adverse Event
Injury
·FENWAL INC.·Product code GKT·December 2, 2011