BEUDAMED
    FDA Adverse Event Other Summary report: N

    VERSACARE BED

    MDR report key: 3170537 · Received June 5, 2013

    Report

    Report Number
    1824206-2013-02978
    Event Type
    Other
    Date Received
    June 5, 2013
    Date of Event
    May 15, 2013
    Report Date
    May 15, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT STATED THEY DID NOT KNOW IF THE BRAKES CAME DISENGAGED OR IF BED SLID ON FLOOR, THE ACCOUNT HAS TILE FLOORS. THE TECHNICIAN INVESTIGATED AND THE ACCOUNT STATED THAT DURING AN IN-SERVICE A NURSE ASKED HOW MUCH WEIGHT WOULD IT TAKE TO MOVE THE BED'S FOOT SECTION BECAUSE A LARGE WOMAN OVER (B)(6) POUNDS LEANED ON ONE AND THE BED MOVED AND SHE FELL. THE TECHNICIAN FOUND THE ACCOUNT DID NOT KNOW WHICH BED MIGHT HAVE BEEN INVOLVED; THEY DID NOT HAVE A SERIAL NUMBER AND HAD NO OTHER INFORMATION IN REGARDS TO THIS INCIDENT. THE TECHNICIAN WAS UNABLE TO INSPECT ANY PRODUCT DO TO THE ACCOUNT NOT HAVING ANY INFORMATION.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGES THAT WHEN A LARGE PATIENT PUSHED ON THE FOOT END OF THE BED TO GET INTO BED THE BED MOVED AND THE PATIENT FELL. THE ACCOUNT STATED THE PATIENT WAS NOT INJURED DUE TO THE FALL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    249459 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1 Other