BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZOOM CRITICAL CARE BED

    MDR report key: 1243185 · Received November 10, 2008

    Report

    Report Number
    1831750-2008-00151
    Event Type
    Malfunction
    Date Received
    November 10, 2008
    Date of Event
    October 11, 2008
    Report Date
    October 11, 2008
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT POWER CORDS OF XPRT MATTRESSES BEING USED ON MODEL 2040 ZOOM CRITICAL CARE BEDS WERE BEING PINCHED AND SOMETIMES FRAYED, AS A RESULT OF THE POWER CORD BEING CAUGHT IN BETWEEN THE OPTIONAL FOOT EXTENDER AND THE FOOTEND OF THE BED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOOM CRITICAL CARE BED AC POWERED HOSP BED FNL STRYKER CORP., MEDICAL DIVISION 2040 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK