BEUDAMED
    FDA Adverse Event Summary report: N

    HNE HEALTHCARE

    MDR report key: 86682 · Received June 28, 1996

    Report

    Report Number
    86682
    Date Received
    June 28, 1996
    Manufacturer
    HNE HEALTHCARE
    Product Code
    JOW
    Report Source
    User Facility report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PT WITH PERIPHERAL VASCULAR DISEASE, WHO HAD BEEN RECEIVING EPIDURAL BUPIVICAINE, COMPLAINED OF RIGHT LOWER EXTREMITY SWELLING AND PAIN AFTER USE OF THE SEQUENTIAL COMPRESSION DEVICE. THE PT DEVELOPED A BRUISE AND BLISTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HNE HEALTHCARE SEQUENTIAL COMPRESSION DEVICE JOW HNE HEALTHCARE AC 500/DVT *

    Patients

    Seq Age Sex Outcome Treatment
    1 *