BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MECTALIF IMPLANT REMOVER

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·March 27, 2014

    TAPERLOC COMPLETE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·February 9, 2026

    TPRLC 133 MP TYPE1 BM SO 9.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 27, 2018

    ALINITY I ANTI-HBC II REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LOM·November 5, 2020

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 14, 2013

    COULTER LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 24, 2014

    JELCO

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code FOZ·May 31, 2011

    TAPERLOC COMPLETE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 8, 2025