401 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DRILL, TRI-FLAT T2 FEMUR Ø4,2X340 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code HWE·October 26, 2015
DE PUY
FDA Adverse Event
Malfunction
·DE PUY·Product code HRS·February 19, 2004
DE PUY
FDA Adverse Event
Other
·DE PUY, INC.·Product code JDO·February 9, 1994
DE PUY
FDA Adverse Event
Death
·*·Product code LXH·May 31, 2005
DE PUY
FDA Adverse Event
Injury
·DE PUY MFG.·Product code KWB·November 8, 1996
DE PUY
FDA Adverse Event
Injury
·DE PUY·Product code KWB·October 10, 2006
V40 COCR LFIT HEAD 36MM/+5
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·May 19, 2020
DEPUY PINNACLE
FDA Adverse Event
Injury
·J&J DEPUY·Product code KWA·December 2, 2013
DE PUY MFG.
FDA Adverse Event
Injury
·DE PUY MFG.·Product code KWB·February 12, 1997
GLENOID-DE PUY
FDA Adverse Event
Malfunction
·DEPUY, INC.·Product code KYM·June 15, 1998
PROFEMUR(R) MODULAR FEMORAL NECK
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code LWJ·February 7, 2017
CONSERVE(R) PLUS HA CUP
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code KWA·February 3, 2017
DE PUY ORTHO TECHNOLOGY
FDA Adverse Event
Other
·DEPUY ORTHOPAEDICS, INC.·Product code HTO·December 1, 1999
DEPUY
FDA Adverse Event
Injury
·DE PUY·Product code LPH·December 5, 2003
PINNACLE METAL INSERT
FDA Adverse Event
Injury
·DE PUY·Product code KWA·August 25, 2014
TIMAX
FDA Adverse Event
Malfunction
·DUPUY MITEK, A JOHNSON AND JOHNSON COMPANY·Product code HWC·November 3, 2005
EXETER V40 STEM 37.5MM NO 0
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CAEN·Product code KWY·May 31, 2006
UNIDENTIFIED ASR TAPER SLEEVE
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. ¿ 8010379·Product code KWY·December 22, 2015
UNKNOWN HIP ACETABULAR LINERS
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 8, 2024
UNK - CONSTRUCTS: LCP DISTAL FEMUR PLATE/SCREWS
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HRS·November 29, 2023