BEUDAMED
    FDA Adverse Event Other Summary report: N

    TOTALCARE

    MDR report key: 1734283 · Received June 21, 2010

    Report

    Report Number
    1824206-2010-08355
    Event Type
    Other
    Date Received
    June 21, 2010
    Date of Event
    May 25, 2010
    Report Date
    May 25, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT DID NOT HAVE A SPECIFIC BED TO INSPECT AND THE SERIAL NUMBER WAS NOT RECORDED. THE WOUND NURSE STATED THAT THE BED WAS OPERATING CORRECTLY BUT THE NURSES ARE UNHAPPY WITH THE FRICTION BETWEEN THE PATIENT AND THE TICKING. THE NURSES USED THE 'BOOST' FUNCTION, BUT STILL ALLEGE THE PATIENT IS DIFFICULT TO PULL UP IN BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT A NURSE HAD INJURED HER SHOULDER WHILE PULLING A PATIENT UP IN THE BED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK