BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACRE BED

    MDR report key: 3061533 · Received March 27, 2013

    Report

    Report Number
    1824206-2013-01719
    Event Type
    Malfunction
    Date Received
    March 27, 2013
    Date of Event
    March 1, 2013
    Report Date
    March 1, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH REPLACED THE PENDANT TO RESOLVE ISSUE WITH BED.

    Description of Event or Problem · 1

    THE TECH ALLEGED THAT THE PENDANT CORD IS DAMAGED AND BARE METAL WIRES ARE EXPOSED. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    124911 VERSACRE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1