2,250 results · 42ms · Sources: EU EUDAMED, US FDA

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HEARTSTART

FDA Adverse Event
Death ·PHILIPS NORTH AMERICA LLC·Product code MKJ·February 17, 2023

PRIDE MOBILITY PRODUCTS

FDA Adverse Event
Injury ·PRIDE MOBILITY PRODUCTS·Product code ITI·August 1, 2023

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 17, 2020

HEARTSTART XL+ DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 28, 2020

HEARTSTART XL+ DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 23, 2019

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 6, 2019

EFFICIA DFM100

FDA Adverse Event
Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC.·Product code MKJ·August 29, 2022

EFFICIA DFM100

FDA Adverse Event
Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC.·Product code MKJ·October 13, 2022

HEARTSTART MRX -EMS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 27, 2018

EFFICIA DFM100

FDA Adverse Event
Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC.·Product code MKJ·March 23, 2023

ALARIS SYSTEM

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code CCK·September 26, 2025

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 1, 2017

EFFICIA DFM100

FDA Adverse Event
Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC·Product code MKJ·August 23, 2022

EFFICIA DFM100 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC.·Product code MKJ·March 19, 2022

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 23, 2019

EFFICIA DFM100

FDA Adverse Event
Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC.·Product code MKJ·July 6, 2023

HEARTSTART MRX -EMS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 10, 2019

EFFICIA DFM100

FDA Adverse Event
Malfunction ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC.·Product code MKJ·July 24, 2023

HEARTSTART XL+ DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MKJ·July 2, 2021

POWERHEART G5 SEMI AUTOMATIC AED

FDA Adverse Event
Malfunction ·CARDIAC SCIENCE CORPORATION·Product code MKJ·May 7, 2026