BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BASIC CONFIGURATION MODEL 6100 BASE

    MDR report key: 1982311 · Received January 13, 2011

    Report

    Report Number
    1831750-2011-00471
    Event Type
    Malfunction
    Date Received
    January 13, 2011
    Date of Event
    December 15, 2010
    Report Date
    December 16, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO THE SALES REPRESENTATIVE FROM THE EMERGENCY SERVICES THAT DURING TRANSFER OF THE PATIENT FROM THE COT INTO THE BED, IT WAS NOT POSSIBLE TO LOCK THE HEIGHT ADJUSTMENT AT THE HEAD END OF THE COT AT THE SECOND HIGHEST LEVEL. HE FURTHER STATES THAT NOBODY WAS IMPAIRED AND THAT THE COT WAS TAKEN OUT OF SERVICE IMMEDIATELY. THERE ARE NO REPORTED ADVERSE CONSEQUENCES.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1