BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TC BARIATRIC PLUS BED

    MDR report key: 3062645 · Received March 19, 2013

    Report

    Report Number
    1824206-2013-01510
    Event Type
    Malfunction
    Date Received
    March 19, 2013
    Date of Event
    February 18, 2013
    Report Date
    February 18, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN THAT DID THE BED SWAP ALSO FOUND THAT THE HEAD SECTION WOULD NOT GO UP. WHEN THE SERVICE TECHNICIAN DID THE BED REPAIR HE FOUND THAT THE HEAD SECTION FUNCTIONED TO SPECIFICATIONS. THE SERVICE TECHNICIAN FOUND THE KNEE UP WAS NOT FUNCTIONING. THE SERVICE TECHNICIAN REPLACED THE KNEE UP VALVE AND THE BED FUNCTIONED TO SPECIFICATIONS.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE HEAD SECTION WOULD NOT GO UP. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    113078 TC BARIATRIC PLUS BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1840

    Patients

    Seq Age Sex Outcome Treatment
    1