15 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
UNK HIP FEMORAL STEM SUMMIT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 13, 2022
UNK KNEE TIBIAL INSERT SIGMA
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 13, 2022
UNK HIP FEMORAL SLEEVE ASR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·September 13, 2022
UNK HIP ACETABULAR CUP ASR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·September 13, 2022
UNK KNEE TIBIAL TRAY SIGMA
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 13, 2022
UNK HIP FEMORAL HEAD METAL ASR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·September 13, 2022
UNK KNEE FEMORAL SIGMA CR
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 13, 2022
PINNACLE SECTOR II CUP 56MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·June 9, 2021
PINN MAR +4 10D 36IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·June 9, 2021
BACTISEAL CATHETER
FDA Adverse Event
Injury
·Product code JXG·October 18, 2017
SROM MARATHON LINER M 28 10DEG
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 8, 2021
VITROS 7% BSA
FDA Adverse Event
Injury
·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code DCF·April 17, 2025
VITROS 5600 INTEGRATED SYSTEM
FDA Adverse Event
Injury
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·November 15, 2013
VITROS 5600 INTEGRATED SYSTEM
FDA Adverse Event
Injury
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·November 15, 2013
VITROS 5600 INTEGRATED SYSTEM
FDA Adverse Event
Injury
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·November 15, 2013