4 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ATTUNE MEDIAL DOME PAT 41MM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·June 5, 2023
UNKNOWN DEPUY TIBIAL INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·April 21, 2014
ASR UNI FEMORAL IMPL SIZE 43
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·September 26, 2012
XACT CAROTID STENT SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NIM·July 15, 2010