BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OEC-DIASONICS C-ARM

    MDR report key: 17385 · Received September 13, 1994

    Report

    Report Number
    17385
    Event Type
    Injury
    Date Received
    September 13, 1994
    Date of Event
    August 23, 1994
    Report Date
    September 13, 1994
    Manufacturer
    OEC-DIASONICS, INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    User Facility report

    Narratives

    Description of Event or Problem · 1

    PT SCHEDULED TO HAVE REPAIR OF HIP FRACTURE. CANCELLED BECAUSE C-ARM WOULD NOT PROVIDE VISUALIZATION. MFR CALLED AND REPLACED BAD MICROPROCESSOR ON ONE OF THE MONITOR CONTROLLER BOARDS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OEC-DIASONICS C-ARM JAA OEC-DIASONICS, INC. 9000

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Hospitalization PT HAD HIP REPAIR RESCHEDULED FOR 8/26/94.