19 results
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35ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·May 16, 2018
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 2, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 14, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 14, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 14, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 16, 2009
CLEARGLIDE EVH LONGVIEW W/SCIS
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 23, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 16, 2009
CLEARGLIDE EVH SMALL W/SCISSOR
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·October 16, 2009
CLEARGLIDE EVH LONGVIEW W/SCIS
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 9, 2009
BIOPSY GUIDE
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·February 11, 2011
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 24, 2009
CLEARGLIDE EVH SMALL W/SCISSOR
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 3, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 16, 2009
PROGREAT
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DQO·March 5, 2024
TERUMO PROGREAT CATHETER
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQO·February 6, 2023
PROGREAT CATHETER
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DQO·January 6, 2024
PROGREAT
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQO·April 15, 2025
BD VACUTAINER® PLUS PLASTIC WHOLE BLOOD TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·June 25, 2018