BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRAUMA STRETCHER

    MDR report key: 2150238 · Received June 10, 2011

    Report

    Report Number
    1831750-2011-05788
    Event Type
    Malfunction
    Date Received
    June 10, 2011
    Date of Event
    May 13, 2011
    Report Date
    May 13, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD OF THE STRETCHER WOULD NOT RAISE. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRAUMA STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1020 NA

    Patients

    Seq Age Sex Outcome Treatment
    1