BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LUMEX EXTRA WIDE CLINICAL CARE RECLINER

    MDR report key: 830992 · Received March 21, 2007

    Report

    Report Number
    MW1042314
    Event Type
    Injury
    Date Received
    March 21, 2007
    Date of Event
    March 2, 2007
    Report Date
    March 21, 2007
    Manufacturer
    GRAHAM-FIELD HEALTH PRODUCTS, INC.
    Product Code
    BYN
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PATIENT WAS SEATED IN A CARDIAC CHAIR-RECLINER TYPE- WHEN SHE ATTEMPTED TO STAND AND GOT HER RIGHT LEG CAUGHT IN THE CHAIR BETWEEN THE FOOT REST AND THE SEAT CUSHION. THE PATIENT HAS A LEFT ABOVE THE KNEE AMPUTATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LUMEX EXTRA WIDE CLINICAL CARE RECLINER CARDIAC CHAIR BYN GRAHAM-FIELD HEALTH PRODUCTS, INC. 587W247 *

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Hospitalization| S