BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2896071 · Received November 20, 2012

    Report

    Report Number
    1824206-2012-07595
    Event Type
    Malfunction
    Date Received
    November 20, 2012
    Date of Event
    October 31, 2012
    Report Date
    October 31, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT FOUND AN INTERNAL SHORT IN THE PT HAND PENDANT. THE ACCOUNT DISCONNECTED THE PT HAND PENDANT TO RESOLVE THE ISSUE. THEY DID NOT WANT THE PT HAND PENDANT REPLACED AT THIS TIME.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE HEAD SECTION WILL GO DOWN INTERMITTENTLY ON ITS OWN AFTER THE HEAD OF THE BED IS RAISED. 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