13 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
VC10 PUMP, 115V
FDA Adverse Event
Malfunction
·GYRUS ACMI, INC.·Product code HHK·January 2, 2025
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·October 14, 2014
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013
SPINAL INJECTION SYSTEM
FDA Adverse Event
Malfunction
·LAURIMED LLC·Product code BSP·June 27, 2008
INTERJECT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FCG·May 27, 2025
CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 14, 2017
CANTATA 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·November 17, 2017
CANTATA 2.5 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·September 17, 2018
CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·September 11, 2018
CANTATA 2.5 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·July 28, 2017
CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·June 15, 2017
CANTATA 2.5 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·May 30, 2018
CANTATA 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·September 6, 2018