61 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
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