10 results
·
32ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ALTIUS SYSTEM
FDA Adverse Event
Malfunction
·NEUROS MEDICAL INC.·Product code LGW·April 2, 2025
ALTIUS SYSTEM
FDA Adverse Event
Malfunction
·NEUROS MEDICAL INC.·Product code LGW·June 20, 2025
PULSE GEN MODEL 104
FDA Adverse Event
Injury
·CYBERONICS INC·Product code LYJ·November 12, 2008
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 31, 2011
XPANDER II IBT
FDA Adverse Event
Malfunction
·KYPHON NEUCHATEL·Product code HRX·July 16, 2013
UNKNOWN ENDO GIA INSTRUMENT
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code GDW·September 14, 2023
AUTO SUTURE
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code GCJ·July 21, 2023
ENDO GIA
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·August 16, 2023
ENDO GIA ULTRA
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code GDW·January 12, 2023
UNKNOWN SIGNIA EGIA ADAPTER
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·January 30, 2023