19 results · 35ms · Sources: EU EUDAMED, US FDA

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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