BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2920286 · Received December 17, 2012

    Report

    Report Number
    1824206-2012-08253
    Event Type
    Malfunction
    Date Received
    December 17, 2012
    Date of Event
    November 28, 2012
    Report Date
    November 28, 2012
    Manufacturer
    HILL-ROM INC
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICAN REPLACED THE HI-LO ASSEMBLY COIL CABLE TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE TECHNICIAN ALLEGED THE COIL CABLE WAS DAMAGED WITH THE BARE METAL WIRES EXPOSED. 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