BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2863400 · Received November 1, 2012

    Report

    Report Number
    1824206-2012-07020
    Event Type
    Malfunction
    Date Received
    November 1, 2012
    Date of Event
    October 12, 2012
    Report Date
    October 12, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH FOUND THE FUSE BLOWN, AND THE COIL CABLE SCUFFED WITH BARE METAL WIRES EXPOSED. THE TECH REPLACED THE FUSE AND THE COIL CABLE TO RESOLVE THE ISSUES.

    Description of Event or Problem · 1

    THE TECH ALLEGED THAT THE CAREGIVER FUNCTIONS ARE NOT FUNCTIONING. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1