63 results · 37ms · Sources: EU EUDAMED, US FDA

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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