1,800 results · 38ms · Sources: EU EUDAMED, US FDA

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2.7MM VA LCK SCREW SLF-TAP

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 21, 2022

2.7MM VA LCK SCREW SLF-TAP

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 21, 2022

2.7MM VA LCK SCREW SLF-TAP

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 12, 2022

2.7MM VA LCK SCREW SLF-TAP

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 12, 2022

BIO-COMP-SITE P-LCK 2.9X15.5MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MAI·June 6, 2022

MOD ARTHRO 5 DEG LCK COLLAR

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HSB·June 7, 2021

VG CR MONO-LCK BRG 12X75

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·October 18, 2017

BIO-COMP-SITE P-LCK 2.9X15.5MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MAI·July 19, 2024

BIO-COMP-SITE P-LCK 2.9X15.5MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MAI·September 19, 2024

4.5MM LCK COMP PL 10H 193MM

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code HRS·October 12, 2018

2.7MM VA LCK SCREW SLF-TAP

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·October 29, 2018

3.5MM LCK TUBULAR PL 6H 82MM

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code HRS·October 30, 2018

4.5MM LCK COMP PL 12H 229MM

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code HRS·December 19, 2018

2.7MM VA LCK SCREW SLF-TAP

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·October 29, 2018

BIO-COMP-SITE P-LCK 2.9X15.5MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MAI·November 13, 2025

VANGUARD CR MONO-LCK BEARING 10X71

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·March 8, 2013

2.7MM VA LCK SCREW SLF-TAP

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·October 29, 2018

MINICTH VSYS/PRT/LCK 4NDL LWPF

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY US SURGICAL·Product code LJT·April 25, 2013

BIO-COMP-SITE P-LCK 2.9X15.5MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MAI·November 13, 2025

BIO-COMP-SITE P-LCK 2.9X15.5MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MAI·October 16, 2025