8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD VACUTAINER PPT PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·May 7, 2018
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018
GALAXY INTRAVASCULAR ULTRASOUND SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (CE)·Product code IYO·February 21, 2013
TRIM-IT FIXATION SCREW, 2.7 MM X 30 MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·January 28, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
ANIMAS CORPORATION·Product code LZG·August 1, 2014
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·July 17, 2018