7 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TOTAL ASR FEM IMP SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·June 4, 2014
HEALIX PEEK ORTHOCORD
FDA Adverse Event
Malfunction
·DEPUY MITEK, A JOHNSON & JOHNSON COMPANY·Product code HWC·November 16, 2012
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·September 27, 2010
SEGMENTAL FLUTED STEM EXTENSION
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·July 10, 2024
SEGMENTAL FLUTED STEM EXTENSION
FDA Adverse Event
Injury
·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code LZO·April 2, 2024
SEGMENTAL STEM COLLAR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·April 2, 2024
ZSS DISTAL FEMORAL XT COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·April 2, 2024