BEUDAMED
    FDA Adverse Event Other Summary report: N

    SYNTHES 7.3 CANNULATED SCREW SET

    MDR report key: 51579 · Received November 18, 1996

    Report

    Report Number
    1719045-1996-00010
    Event Type
    Other
    Date Received
    November 18, 1996
    Date of Event
    October 8, 1996
    Report Date
    November 16, 1996
    Manufacturer
    SYNTHES USA
    Product Code
    HWX
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CO'S 7.3 CANNULATED SCREW SET, THE 7.3 CANNULATED TAP SHEARED OFF WHEN SCREWING IN THE BONE SHAFT. LEFT PORTION OF TAP IN BONE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SYNTHES 7.3 CANNULATED SCREW SET Implant TAP HWX SYNTHES USA NA A31L305

    Patients

    Seq Age Sex Outcome Treatment
    1 15 YR Other