BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIG WHEEL STRETCHER

    MDR report key: 724058 · Received June 2, 2006

    Report

    Report Number
    1831750-2006-00037
    Event Type
    Malfunction
    Date Received
    June 2, 2006
    Date of Event
    May 3, 2006
    Report Date
    May 3, 2006
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE STRETCHER BRAKES ALLEGEDLY POPPED OUT OF ENGAGED MODE. NO PATIENT INJURY OR INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIG WHEEL STRETCHER WHEELED HOSPITAL STRETCHER FPO STRYKER CORP., MEDICAL DIV 1015 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Death