BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OHI 540

    MDR report key: 1346815 · Received March 18, 2009

    Report

    Report Number
    MW5010383
    Event Type
    Injury
    Date Received
    March 18, 2009
    Date of Event
    March 10, 2009
    Report Date
    March 18, 2009
    Manufacturer
    OHIO MEDICAL INSTRUMENT CO., PEDIGO PRODUCTS, INC.
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PATIENT LYING ON STRETCHER ATTEMPTED TO REPOSITION HIMSELF ON STRETCHER TO VOID, LEANED AGAINST LEFT SIDERAIL WHEN IT RELEASED AND PATIENT FELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OHI 540 STRETCHER FPO OHIO MEDICAL INSTRUMENT CO., PEDIGO PRODUCTS, INC. K540-001

    Patients

    Seq Age Sex Outcome Treatment
    1 76 YR Other