10,000 results
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54ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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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