61 results · 21ms · Sources: EU EUDAMED, US FDA

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ONE TOUCH ULTRA

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code NBW·November 14, 2005

CLJ INNER TUBE #6 W/TUCKER VALVE

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BTR·November 15, 2010

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·October 1, 2014

PILLING CLJ INNER TUBE #5 W TUCKER VAL

FDA Adverse Event
Malfunction ·TELEFLEX·Product code BTR·April 30, 2012

PILLING CLJ INNER TUBE #5 W/TUCKER VALVE

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BTR·January 29, 2014

GORE® TAG® THORACIC ENDOPROSTHESIS

FDA Adverse Event
Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·September 9, 2021

ENDURANT STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·May 4, 2022

TALENT TAA STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·November 20, 2020

ATLAS PLUS VR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL·Product code LWS·January 23, 2009

BD BACTEC¿ MGIT¿ 960 SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·July 6, 2021

ENDURANT STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·August 25, 2020

VALIANT STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·November 20, 2020

J+J

FDA Adverse Event
Malfunction ·J + J·Product code KWB·October 22, 2002

ENDURANT STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·April 12, 2019

ONYX

FDA Adverse Event
Malfunction ·COVIDIEN (IRVINE)·Product code MFE·June 20, 2017

SYNCHRON DRUG CALIBRATOR 2

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code DLJ·February 17, 2012

SYNCHRON DRUG CALIBRATOR 2

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code DLJ·March 26, 2012

SYNCHRON SYSTEM DRUG CALIBRATOR 2

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code DLJ·March 7, 2012

SYNCHRON SYSTEMS DRUG CALIBRATOR 2

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code DLJ·March 5, 2012

ROCHE

FDA Adverse Event
Malfunction ·ROCHE·Product code DLJ·December 21, 2017