6 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
UNKNOWN·Product code ITJ·June 3, 2013
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 21, 2011
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·August 28, 2008
G7 ACETABULAR LINER NEUTRAL 36MM E
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code PBI·June 7, 2024
G7 ACETABULAR SYSTEM SHELL 52E
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code PBI·June 7, 2024
G7 ACETABULAR LINER NEUTRAL 36MM F
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code PBI·June 7, 2024