10,000 results · 54ms · Sources: EU EUDAMED, US FDA

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CANCL BONE SCW TI 6.5MMX3

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWC·February 25, 2026

CANCL BONE SCW TI 6.5MMX3

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWC·February 25, 2026

CANCL BONE SCW TI 6.5MMX2

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWC·February 25, 2026

20 MM LENGTH X 6.5 MM TI FULLY THREADED CANCELLOUS BONE SCREW

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWC·March 24, 2026

35 MM LENGTH X 6.5 MM TI FULLY THREADED CANCELLOUS BONE SCREW

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWC·March 24, 2026

35 MM LENGTH X 6.5 MM TI FULLY THREADED CANCELLOUS BONE SCREW

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWC·March 24, 2026

30 MM LENGTH X 6.5 MM TI FULLY THREADED CANCELLOUS BONE SCREW

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWC·March 24, 2026

VIPER SYSTEM POLY SCREWDRIVER SHAFT, CANN

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·October 28, 2022

VIPER SYSTEM POLY SCREWDRIVER SHAFT, CANN

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·October 28, 2022

VIPER SYSTEM POLY SCREWDRIVER SHAFT, CANN

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·October 28, 2022

VIPER SYSTEM POLY SCREWDRIVER SHAFT, CANN

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·October 28, 2022

VIPER SYSTEM POLY SCREWDRIVER SHAFT, CANN

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·October 28, 2022

POLY SCW DRIVER SHFT, CANNULTD

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·April 6, 2021

POLY SCW DRIVER SHFT, CANNULTD

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·July 2, 2020

VIPER SYSTEM POLY SCREWDRIVER SHAFT, CANN

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·June 22, 2020

REGENEREX ACET SHELL 64ODX54ID

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 31, 2018

ARCOS 14X250MM SPL TPR DIST HA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 31, 2018

UNKNOWN HEAD

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 4, 2018

HWAL ARCOMXL ALLPOLY 36IDX52OD

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 31, 2018

ARCOS CON SZ A HI 50MM HA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 31, 2018