7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ASR ACETABULAR IMPLANT 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·October 9, 2012
TOTAL ASR FEM IMP SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·October 9, 2012
68MM CUP SIZE REVISION SHELL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·May 23, 2025
NAV 5.5MM TAP (CANNULATED)
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·March 13, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·August 12, 2014
PFC KEEL TIB TRAY CEM SZ4
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 18, 2011
EVOLUT FX PLUS VALVE
FDA Adverse Event
Malfunction
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 3, 2025