BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRETCHER

    MDR report key: 1811459 · Received August 17, 2010

    Report

    Report Number
    1831750-2010-01851
    Event Type
    Malfunction
    Date Received
    August 17, 2010
    Date of Event
    July 20, 2010
    Report Date
    July 20, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE STRETCHER COULD NOT BE PUMPED UP ON THE FOOT END.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV 1080 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA