BEUDAMED
    FDA Adverse Event Other Summary report: N

    TOTALCARE

    MDR report key: 1304787 · Received February 3, 2009

    Report

    Report Number
    1824206-2009-00468
    Event Type
    Other
    Date Received
    February 3, 2009
    Date of Event
    January 5, 2009
    Report Date
    January 5, 2009
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE FACILITIES BIOMED STATED THAT THE BATTERY LIGHT WAS ON, BUT HE DID NOT KNOW HOW TO USE THE BATTERY BACK UP. TECHNICAL SUPPORT WALKED THE BIOMED THROUGH THE BATTERY BACK UP PROCESS AND ALL OF THE BED FUNCTIONS WORKED. A HILL-ROM TECHNICIAN INVESTIGATED AND FOUND THE BACK-UP BATTERY LIGHT WAS ILLUMINATED WHEN BED WAS UNPLUGGED AND BACK-UP BATTERY FUNCTIONS OPERATED CORRECTLY. THE TECHNICIAN INDICATED THAT THE BACK-UP BATTERY IS BECOMING WEAK AND IS 3 YEARS OLD, BUT IT IS STILL FUNCTIONAL. THE FACILITY DID NOT HAVE A PM SCHEDULE FOR THE BEDS. THE FACILITIES STAFF DECLINED TO RELEASE INFORMATION REGARDING THE INCIDENT.

    Description of Event or Problem · 1

    ALLEGED A PATIENT CODED IN THE BED DURING TRANSPORT. THE NURSE SAID THE POWER CORD WAS CAUGHT IN THE CASTERS AND THE BATTERY BACK-UP WOULD NOT WORK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1900

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK