BEUDAMED
    13 results · 44ms · Sources: EU EUDAMED, US FDA

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    POINTED REDUCTION FORCEPS

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·February 7, 2022

    VAL SCREW, TI, 1.6 X 9MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·December 21, 2020

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·December 21, 2020

    VAL SCREW, TI, 1.6 X 10MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·December 21, 2020

    DRIVER SHAFT, T6, NON-RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 17, 2024

    SOLID SCREWDRIVER, T6 HEXALOBE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 17, 2024

    DRIVER SHAFT, T6, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 17, 2024

    DRIVER SHAFT, T6, NON-RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 17, 2024

    DRIVER SHAFT, T6, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 17, 2024

    POINTED REDUCTION FORCEPS

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 17, 2024

    ILS 25MM CURVED

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 12, 2014

    SPECTRAFLEX

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2010

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·December 12, 2012