7 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
RESOLUTE ONYX RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·January 31, 2019
RESOLUTE INTEGRITY RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·April 9, 2019
LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·September 25, 2018
BLACKMAX-NEURO
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HSZ·June 10, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011
JAGWIRE GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EZB·September 12, 2008
SYRINGE 10ML SALINE XS
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND CO.·Product code FMF·December 10, 2020