BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RECOVERCARE

    MDR report key: 3811802 · Received May 9, 2014

    Report

    Report Number
    MW5036075
    Event Type
    Malfunction
    Date Received
    May 9, 2014
    Date of Event
    April 30, 2014
    Report Date
    May 8, 2014
    Manufacturer
    RECOVERCARE
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PATIENT WAS BEING PLACED BACK INTO THE BED BY PT WHEN IT BEGAN PULSING UP AND DOWN. THE BED FRAME THEN WENT INTO POSITION WHERE THE FOOT OF THE BED WAS ALL THE WAY DOWN TO THE FLOOR, AND THE HEAD OF THE BED UPRIGHT; AS IF THE PATIENT WAS GOING INTO A STANDING POSITION. THE PT IMMEDIATELY UNPLUGGED THE BED WHILE THE OTHER PT ENSURED THE PATIENT'S SAFETY. THE PT KNEW TO IMMEDIATELY PULL THE MANUAL LEVER FROM BENEATH THE BED AND INSERT IT INTO THE APPROPRIATE LOCATION AT THE TOP OF THE BED FOR MANUAL CRANK BACK INTO POSITION. PATIENT WAS UNHARMED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    282098 RECOVERCARE HI-LO BED FNL RECOVERCARE UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 81 YR