BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OEM STRETCHER CONFIGURATIONS

    MDR report key: 1945337 · Received December 27, 2010

    Report

    Report Number
    1831750-2010-05175
    Event Type
    Malfunction
    Date Received
    December 27, 2010
    Date of Event
    November 29, 2010
    Report Date
    November 29, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END OF STRETCHER DRIFTS DOWN. A DECEASED PT WAS ON THE STRETCHER AND WAS REPORTED THE BODY SLID OFF THE STRETCHER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OEM STRETCHER CONFIGURATIONS HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV. 0722 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK