BEUDAMED
    FDA Adverse Event Other Summary report: N

    HOSPITAL BED

    MDR report key: 1842573 · Received September 16, 2010

    Report

    Report Number
    2182305-2010-00035
    Event Type
    Other
    Date Received
    September 16, 2010
    Date of Event
    August 5, 2010
    Report Date
    September 2, 2010
    Manufacturer
    JOERNS HEALTHCARE
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO MANUFACTURER, BY DOUGLAS MEDICAL; FOR A (B)(4), PER CARE PROVIDER, THE BED WAS MAKING A NOISE WHEN RAISING, SO SHE CALLED DOUGLAS MEDICAL TO REPAIR. THE ADULT FOSTER CARE PROVIDER GOT UNDER THE BED TO SEE WHAT WAS MAKING THE NOISE WHEN THE END OF THE BED DROPPED DOWN ON HER HAND, HER MIDDLE FINGER GOT BROKEN. "THIS ADULT CARE PROVIDER STATED SHE SHOULD HAVE KNOWN BETTER THAT TO GET UNDER THE BED WHEN HEARING A NOISE". (B)(4) TO GET BED BACK FOR EVALUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HOSPITAL BED HOSPIATL BED, ELECTRIC FNL JOERNS HEALTHCARE U770

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other