401 results · 30ms · Sources: EU EUDAMED, 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