BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 2902941 · Received November 29, 2012

    Report

    Report Number
    1824206-2012-07777
    Event Type
    Malfunction
    Date Received
    November 29, 2012
    Date of Event
    November 8, 2012
    Report Date
    November 8, 2012
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD WILL NOT LOWER ELECTRICALLY OR WITH CARDIO PULMONARY RESUSCITATION. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 852

    Patients

    Seq Age Sex Outcome Treatment
    1