BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    GLENOID INSERTER/IMPACTOR, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 1, 2025

    GLENOID INSERTER/IMPACTOR, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 6, 2024

    GLENOID INSERTER/IMPACTOR, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 20, 2025

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·January 22, 2013

    ANGLED REAMER, DRIVE SHAFT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 17, 2023

    ANGLED REAMER SLEEVE, 10°

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 17, 2023