BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BASIC CONFIGURATION MODEL 6100 BASE

    MDR report key: 2232699 · Received July 19, 2011

    Report

    Report Number
    1831750-2011-07339
    Event Type
    Malfunction
    Date Received
    July 19, 2011
    Date of Event
    June 17, 2011
    Report Date
    June 21, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    ---
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION UNDERWAY.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE COT COLLAPSED DOWN TO THE LOWER POSITION. THERE WAS NO REPORTED PT INVOLVEMENT OR ADVERSE CONSEQUENCES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BASIC CONFIGURATION MODEL 6100 BASE STRETCHER, WHEELED --- STRYKER MEDICAL 6100 NA

    Patients

    Seq Age Sex Outcome Treatment
    1