BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PULSATILE ANTI-EMBOLISM STOCKING

    MDR report key: 30027 · Received February 12, 1996

    Report

    Report Number
    MW1008316
    Event Type
    Injury
    Date Received
    February 12, 1996
    Date of Event
    January 25, 1996
    Report Date
    February 7, 1996
    Manufacturer
    BAXTER HEALTHCARE CORP.
    Product Code
    JOW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    BAXTER HEALTHCARE CORP, 1430 WAUKEGAN RD, MCGAW PARK, IL 60085-6787. BASED ON THE INFO PROVIDED IN THE MEDWATCH REPORT AND ON INFO FROM THE RPTR, WE HAVE DETERMINED THAT THIS EVENT IS NOT REPORTABLE UNDER THE MEDICAL DEVICE REPORTING REGULATIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PULSATILE ANTI-EMBOLISM STOCKING ANTI-EMBOLISM STOCKING JOW BAXTER HEALTHCARE CORP.

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR Required Intervention USED WITH AIR PUMP UNIT FOR INTERMITTENT LIMB| COMPRESSION TO PREVENT DEEP VEIN THROMBOSIS.