9 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ON-X PROSTHETIC HEART VALVE
FDA Adverse Event
Injury
·ON-X LIFE TEHCNOLOGIES, INC.·Product code DYE·January 14, 2016
ON-X MITRAL PROSTHETIC HEART VALVE
FDA Adverse Event
Other
·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·July 14, 2011
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 27, 2014
RSVR MMT-326A 10PK PRDGM 1.8ML 13L
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code FMF·November 8, 2010
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·December 26, 2012
ONX AORTIC ANATOMIC EXT 27/29
FDA Adverse Event
Injury
·ONX LIFE TECHNOLOGIES, INC.·Product code LWQ·March 14, 2017
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·August 13, 2024
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·July 11, 2023
ONX AORTIC ANATOMIC EXT 23
FDA Adverse Event
Injury
·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·August 26, 2020