BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CUB PEDIATRIC CRIB-HYD BASE

    MDR report key: 2243261 · Received September 1, 2011

    Report

    Report Number
    1831750-2011-09378
    Event Type
    Malfunction
    Date Received
    September 1, 2011
    Date of Event
    August 8, 2011
    Report Date
    August 8, 2011
    Manufacturer
    FLEXTRONICS EMS CANADA
    Product Code
    FMS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS - PCB SCALE BOARD.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SCALE WAS INACCURATE. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CUB PEDIATRIC CRIB-HYD BASE A/C HOSPITAL BED FMS FLEXTRONICS EMS CANADA FL19H NA

    Patients

    Seq Age Sex Outcome Treatment
    1