BEUDAMED
    FDA Adverse Event Other Summary report: N

    VERSACARE BED

    MDR report key: 2211367 · Received August 3, 2011

    Report

    Report Number
    1824206-2011-04091
    Event Type
    Other
    Date Received
    August 3, 2011
    Date of Event
    June 26, 2011
    Report Date
    July 7, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE FIELD TECH WAS UNABLE TO EXAMINE THE BED, AS THE FACILITY DOES NOT KNOW WHICH BED WAS INVOLVED IN THE EVENT. THE ACCOUNT WOULD NOT PROVIDE ANY ADD'L INFO NOR ALLOW WITNESSES TO BE INTERVIEWED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES TWO STAFF MEMBERS WERE MOVING AN EMPTY BED, ONE AT THE HEAD END, THE OTHER AT THE FOOT OF THE BED. THE STAFF MEMBER WHO WAS AT THE FOOT OF THE BED INDICATED THAT ONCE THE BED GOT MOVING IT ACTUALLY GAINED MOMENTUM. NOT PREPARED FOR THIS, THE STAFF'S FOOT GOT CAUGHT UNDER THE LOW BED FRAME AND WAS PULLED FOR A BIT UNTIL THE BED FINALLY CAME TO STOP. AFTER THE SHIFT, THE STAFF MEMBER'S PAIN GOT WORSE AND THEY WENT TO A DOCTOR. THE STAFF MEMBER STRAINED THEIR THIGH AND CALL AND WILL BE OFF WORK FOR THE REMAINDER OF THE WEEK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK