468 results
·
42ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
MAQUET INC.
FDA Adverse Event
Malfunction
·MAQUET, INC.·Product code CBK·April 12, 2011
GETINGE/CASTLE
FDA Adverse Event
Malfunction
·MAQUET, INC.·Product code FQO·April 1, 2010
CASTLE
FDA Adverse Event
Malfunction
·MAQUET, INC. (F.K.A. GETINGEUSA)·Product code FSY·January 15, 2010
8010042-2007-00153
FDA Adverse Event
Malfunction
·Product code CBK·July 6, 2007
*
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·May 28, 2008
8010042-2008-00045
FDA Adverse Event
Malfunction
·Product code CBK·April 4, 2008
8010042-2008-00046
FDA Adverse Event
Malfunction
·Product code CBK·April 4, 2008
8010042-2008-00044
FDA Adverse Event
Malfunction
·Product code CBK·April 4, 2008
8010042-2008-00014
FDA Adverse Event
Malfunction
·Product code CBK·February 20, 2008
8010042-2008-00022
FDA Adverse Event
Malfunction
·Product code CBK·February 26, 2008
8010042-2008-00041
FDA Adverse Event
Malfunction
·Product code CBK·March 27, 2008
8010762-2008-00001
FDA Adverse Event
Malfunction
·Product code DTQ·February 20, 2008
8010042-2008-00024
FDA Adverse Event
Malfunction
·Product code CBK·February 15, 2008
8010042-2008-00019
FDA Adverse Event
Malfunction
·Product code CBK·February 20, 2008
ROTAFLOW CENTRIFUGAL PUMP
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code DWA·November 9, 2006
8010042-2008-00047
FDA Adverse Event
Malfunction
·Product code IOY·April 11, 2008
8010042-2008-00050
FDA Adverse Event
Malfunction
·Product code CBK·April 16, 2008
8010042-2008-00029
FDA Adverse Event
Malfunction
·Product code CBK·March 13, 2008
*
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·February 13, 2008
8010042-2008-00031
FDA Adverse Event
Malfunction
·Product code CBK·February 29, 2008