63 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
*
FDA Adverse Event
Malfunction
·STELLATE SYSTEMS·Product code GWQ·March 10, 2010
CABLE 1.0MMX750XX W/CRIMP
FDA Adverse Event
Malfunction
·SYNTHES INC.·Product code JDQ·December 14, 2016
OPTRELL
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DRF·June 27, 2023
SERIES TWENTY THOUSAND LEGACY
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HQE·December 21, 1999
VERSAPULSE POWERSUITE
FDA Adverse Event
Malfunction
·LUMENIS LTD·Product code GEX·September 8, 2022
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·March 5, 2009
UNSPECIFIED BD INTIMA-II NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·June 10, 2020
SYSTEM 6 CHARGER
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·April 21, 2014
STELLANT DUAL INJECTION SYSTEM
FDA Adverse Event
Malfunction
·MEDRAD·Product code DXT·September 13, 2012
UNICEL® DXI 600 ACCESS® IMMUNOASSAY SYSTEM WITH DUAL GANTRY
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·April 29, 2011
MEDRAD STELLANT D INJECTOR SYSTEM
FDA Adverse Event
Malfunction
·MEDRAD·Product code DXT·March 19, 2014
MEDRAD STELLANT CT INJECTION SYSTEM
FDA Adverse Event
Malfunction
·BAYER MEDICAL CARE, INC.·Product code DXT·March 14, 2019
PENUMBRA SYSTEM ACE 68 HI-FLOW KIT
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·February 28, 2017
MEDRAD® STELLANT CT INJECTION SYSTEM
FDA Adverse Event
Malfunction
·BAYER MEDICAL CARE, INC.·Product code DXT·October 11, 2018
MEDRAD STELLANT FLEX CT INJECTION SYSTEM
FDA Adverse Event
Malfunction
·BAYER MEDICAL CARE INC.·Product code IZQ·July 12, 2021
MEDRAD® STELLANT CT INJECTION SYSTEM
FDA Adverse Event
Malfunction
·BAYER MEDICAL CARE, INC.·Product code DXT·January 23, 2019
MEDRAD STELLANT FLEX CT INJECTION SYSTEM
FDA Adverse Event
Malfunction
·BAYER MEDICAL CARE INC.·Product code DXT·January 17, 2025
PINNACLE SECTOR II CUP 54MM
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code KWA·December 7, 2020
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Malfunction
·RICE CREEK MFG·Product code DXY·February 9, 2013
OMNIPOD 5 CONTROLLER
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code QFG·January 23, 2026