9 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
SERO-FUGE 2002 CENTRIFUGE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code LXG·April 24, 2020
MYCARELINK
FDA Adverse Event
Malfunction
·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·May 3, 2018
MYCARELINK
FDA Adverse Event
Malfunction
·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·May 3, 2018
MYCARELINK
FDA Adverse Event
Malfunction
·PLEXUS MANUFACTURING SDN. BHD·Product code NVZ·June 15, 2018
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 28, 2012
AUTO SUTURE
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GAG·September 25, 2013
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NVZ·May 1, 2018
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code NVZ·December 22, 2016
EXTRACTSCR F/PFNA BLADE
FDA Adverse Event
Malfunction
·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code HWB·January 29, 2018