128 results · 27ms · Sources: EU EUDAMED, US FDA

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LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·February 16, 2009

LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·March 3, 2010

REVIVER AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·March 17, 2010

LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·December 12, 2014

LIFELINE VIEW AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·December 22, 2014

LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·July 9, 2015

REVIVER

FDA Adverse Event
Malfunction ·DEFIBTECH LLC·Product code MKJ·July 2, 2024

RMU-2000 ARM XR CHEST COMPRESSION DEVICE

FDA Adverse Event
Malfunction ·DEFIBTECH LLC.·Product code DRM·August 29, 2024

LIFELINE

FDA Adverse Event
Malfunction ·DEFIBTECH LLC·Product code DRM·August 1, 2024

LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·November 17, 2009

LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·November 5, 2008

LIFELINE, AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·December 31, 2008

LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·December 16, 2008

REVIVER

FDA Adverse Event
Malfunction ·DEFIBTECH LLC·Product code MKJ·April 18, 2024

LIFELINE

FDA Adverse Event
Malfunction ·DEFIBTECH LLC·Product code MKJ·June 19, 2024

LIFELINE

FDA Adverse Event
Malfunction ·DEFIBTECH LLC·Product code MKJ·April 26, 2024

LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·October 8, 2010

DEFIBTECH REVIVER AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·April 22, 2005

LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·October 22, 2008

LIFELINE AED

FDA Adverse Event
Malfunction ·DEFIBTECH, LLC·Product code MKJ·October 22, 2008