BEUDAMED
    FDA Adverse Event Other Summary report: N

    ELECTRIC HOSPITAL BED

    MDR report key: 703142 · Received April 19, 2006

    Report

    Report Number
    2182305-2006-00007
    Event Type
    Other
    Date Received
    April 19, 2006
    Date of Event
    January 24, 2006
    Report Date
    March 24, 2006
    Manufacturer
    OPTIMA HEALTHCARE, INC.
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    HE WAS CALLED TO END USER HOME BECAUSE OF A BED TIPPING. THIS COMPLAINT FIRST WAS ENTERED AS "SALES REP SAID BED IS NOT WORKING PROPERLY, REPLACE UNDER WARRANTY AS A CONCESSION" THEN ON 3/14/06 NEW ENTRY AS "SUPPSEDLY THERE WAS AN INCIDENT WITH THIS BED". END USER STATED THEY COULD NOT GET THE PT OUT OF BED SO THEY WERE ADVISED TO CALL 911. WHEN PRAXAIR ARRIVED THE BED WAS IN THE UPRIGHT POSITION, AND THE BED HAD BEEN MOVED ACROSS THE ROOM FROM WHERE THEY HAD SET IT UP. THE FAMILY STATED THEY MOVED THE BED WITH PT IN IT SO HE COULD VIEW THE TV BETTER. PT WAS NOT INJURED, ANXIETY, HOWEVER PT WAS HANGING FROM THE BED AND 911 WAS CALLED. THE HEAD OF THE BED ON ONE SIDE GAVE AWAY THAT SECTION OF BED TIPPED ON AN ANGLE AND PT WAS CAUGHT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ELECTRIC HOSPITAL BED ELECTRIC BED FNL OPTIMA HEALTHCARE, INC. IC-5310 *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other