48 results
·
78ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·June 12, 2018
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·October 11, 2007
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·October 1, 2007
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·October 1, 2007
LIFEPAK CR(R) PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·October 2, 2007
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·November 20, 2007
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·September 14, 2007
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·September 5, 2007
INTRALASE FS2
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·June 5, 2019
IFS
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·January 7, 2020
IFS
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·January 7, 2020
IFS
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·January 7, 2020
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·August 3, 2022
INTRALASE FS2
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC·Product code HNO·August 24, 2018
HEARTWARE VENTRICULAR ASSIST SYSTEM- BATTERY
FDA Adverse Event
Malfunction
·HEARTWARE, INC.·Product code DSQ·June 25, 2018
3007042319-2018-03303
FDA Adverse Event
Malfunction
·July 27, 2018
HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER AC ADAPTER
FDA Adverse Event
Malfunction
·HEARTWARE, INC.·Product code DSQ·June 29, 2018
HEARTWARE VENTRICULAR ASSIST SYSTEM - BATTERY
FDA Adverse Event
Malfunction
·HEARTWARE, INC.·Product code DSQ·June 6, 2018
HEARTWARE VENTRICULAR ASSIST SYSTEM - BATTERY
FDA Adverse Event
Malfunction
·HEARTWARE, INC.·Product code DSQ·November 14, 2018
O-ARM 1000 IMAGING SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·July 29, 2016