BEUDAMED
    444 results · 54ms · Sources: EU EUDAMED, US FDA

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    FEMORAL STEM, SIZE 3

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC·Product code KWY·August 20, 2003

    DURASUL COCR HEAD 38/ 0 'M' 12/14

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·January 4, 2013

    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

    BONE SCREW SELF-TAPPING 35 MM LENGTH 6.5 MM DIA.

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 15, 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

    SHELL POROUS WITH MULTI HOLES 58 MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025

    XLPE 10 DEG POLY LINER 58X36

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 15, 2025

    BIOLOX® DELTA, CERAMIC FEMORAL HEAD, L, 28/+3.5, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LZO·March 4, 2022

    RETi-LOCK Cluster-Hole Acetabular Shells with Sealed Screw-holes manufactured by Zimmer, Austin, Texas

    FDA Recall
    Terminated ·Centerpulse Orthopedics, Inc·Product code LZO·September 30, 2003

    UNISPACER 54MM X 4MM MED RT

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS, INC.·Product code HSH·January 16, 2004

    ULTRA TIB INS RT SZ1/2 9MM NK II

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS, INC.·Product code HSH·January 30, 2004

    NP FEM LT SZ3 NK II

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS INC.·Product code HSA·January 30, 2004

    COCR CONCENTRIC HUM HD 48MMX17MM SELEC

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS, INC.·Product code KWS·March 16, 2004

    NP FEM LT SZ3 NK II

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS, INC.·Product code HSA·March 16, 2004

    ULTRA TIB INS LT SZ3/4/5 13MM NK II

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS INC.·Product code HSH·January 30, 2004

    CLUSTER-HOLE PRI SHELL W/SEALED SCWHLS

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS, INC.·Product code LZO·February 6, 2004

    TIB B/P SZ4 UNI-KNEE

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS, INC.·Product code HRY·March 30, 2004

    NKII DURASUL CONG TIB INS SZ 1/2, RT, 9MM

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS, INC.·Product code JWH·March 17, 2004