BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FLOWTRON DVT

    MDR report key: 23769 · Received July 3, 1995

    Report

    Report Number
    23769
    Event Type
    Injury
    Date Received
    July 3, 1995
    Date of Event
    May 28, 1995
    Report Date
    June 28, 1995
    Manufacturer
    HNE HEALTHCARE
    Product Code
    JOW
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    NJ, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PT IN HOSP., RECOVERING FROM FX LEFT HIP, FEMUR REPAIR, COMPRESSION DEVICE APPLIED 5/28/95. PT STATES LACK OF MOVEMENT OF RIGHT FOOT. EXAMINED FOOT REVEALED RIGHT FOOT DROP. COMPRESSION WAS REMOVED FROM PT. DIAGNOSIS PERONEAL NERVE PALSY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLOWTRON DVT SEQUENTIAL SUPRESSION DENID JOW HNE HEALTHCARE AC500DVT NA

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Required Intervention