128 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
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