59 results · 30ms · Sources: EU EUDAMED, US FDA

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LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020

LIGASURE

FDA Adverse Event
Injury ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020

LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 16, 2021

LIFEPAK(R) 1000 DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 6, 2014

DIMENSION(R) CLINICAL CHEMISTRY SYSTEM

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code LCP·June 3, 2013

3.7MM CANNULATED LOCKING SCREW

FDA Adverse Event
Death ·SYNTHES MONUMENT·Product code KTT·June 17, 2011

LIGASURE

FDA Adverse Event
Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 14, 2021

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·November 7, 2019

LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 23, 2014