236 results
·
68ms
·
Sources: EU EUDAMED, US FDA
BIOMET ORTHOPEDICS INC
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS, INC·Product code HTY·September 18, 2003
BIOMET ORTHOPEDICS, INC.
FDA Adverse Event
Injury
·BIOMET, INC.·Product code JDI·June 23, 2005
BIOMET ORTHOPEDICS, INC.
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·January 12, 2007
BIOMET ORTHOPEDICS INC
FDA Adverse Event
Injury
·BIOMET, INC.·Product code JDI·January 18, 2008
BIOMET ORTHOPEDICS, INC.
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS, INC.·Product code JWH·January 7, 2008
BIOMET ORTHOPEDICS, INC
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS, INC·Product code HSA·December 12, 2002
BIOMET ORTHOPEDICS, INC
FDA Adverse Event
Injury
·BIOMET ORTHPEDICS, INC·Product code HWC·October 15, 2002
BIOMET ORTHOPEDICS, INC. REPICCI II
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS, INC.·Product code JWH·January 31, 2005
E-POLY 40MM RINGLOC ACETABULAR LINER +3 HI-WALL SIZE 24
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MAY·December 3, 2010
ST GOBAIN
FDA Adverse Event
Other
·CERAMIQUES AVANCEES DESMARQUES·Product code JDI·January 13, 2003
BIOMET ORTHOPEDIC, INC
FDA Adverse Event
Injury
·BIOMET ORTHOPEDIC, INC·Product code JDI·February 22, 2008
VANGUARD CR TIBIA BEARING 10X63/67
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·November 27, 2012
M2A MAGNUM MODULAR HEAD 50MM HEAD DIAMETER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·December 28, 2010
22.2MM DIA COCR MODULAR HEAD -5 NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·September 24, 2013
BIOMET ORTHOPEDICS M2A MAGNUM
FDA Adverse Event
Injury
·BIOMET INC.·Product code KWA·November 9, 2021
ACE LONG TROCANTERIC NAIL RIGHT, 130, 380 MM, 9 DIA
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC·Product code HSB·September 19, 2014
TAPERLOC FEMORAL STEM
FDA Adverse Event
Injury
·BIOMET UK LTD·Product code LPH·December 2, 2010
LONGEVITY CONST LINER 50X28
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWZ·September 16, 2025
BONE SCREW SELF-TAPPING 6.5 MM DIA. 20 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025
BONE SCREW SELF-TAPPING 6.5 MM DIA. 25 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025