BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACUSON

    MDR report key: 4213659 · Received September 26, 2014

    Report

    Report Number
    3009498591-2014-00031
    Event Type
    Malfunction
    Date Received
    September 26, 2014
    Date of Event
    September 18, 2014
    Report Date
    September 26, 2014
    Manufacturer
    SIEMENS MEDICAL SOLUTIONS USA INC.
    Product Code
    IYN
    PMA / PMN Number
    131164
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    A FOLLOW UP REPORT WILL BE SUBMITTED WHEN THE INVESTIGATION HAS BEEN COMPLETED.

    Description of Event or Problem · 1

    THE BOLTS THAT SECURE THE UILK ASSEMBLY TO THE UIC COLUMN HAVE SHEARED, THIS HAS ALLOWED THE UILK ARM TO MOVE AND BECOME UNSTABLE. NO CONSEQUENCES TO THE PT OR USER WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    603038 ACUSON DIAGNOSTIC ULTRASOUND DEVICE IYN SIEMENS MEDICAL SOLUTIONS USA INC. ACUSON SC2000

    Patients

    Seq Age Sex Outcome Treatment
    1