BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CAREASSIST BED

    MDR report key: 1822035 · Received August 26, 2010

    Report

    Report Number
    3006697241-2010-00010
    Event Type
    Malfunction
    Date Received
    August 26, 2010
    Date of Event
    August 2, 2010
    Report Date
    August 2, 2010
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN ASSESSED THE BED AND FOUND THE SCALE BOARD WAS NOT WORKING PROPERLY DUE TO CORROSION CREATING A BAD CONTACT TO THE PODS. THE TECHNICIAN REPLACED THE SCALE BOARD, CALIBRATED THE SCALE AND PERFORMED A FUNCTION CHECK TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THERE WAS NO DISPLAY ON SCALE PODS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CAREASSIST BED AC POWERED HOSPITAL BED FNL HILL-ROM DE MEXICO S DE RL DE CV 1170

    Patients

    Seq Age Sex Outcome Treatment
    1