BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CUB PEDIATRIC CRIB-HYD BASE

    MDR report key: 2923037 · Received December 27, 2012

    Report

    Report Number
    1831750-2012-13360
    Event Type
    Malfunction
    Date Received
    December 27, 2012
    Date of Event
    November 29, 2012
    Report Date
    November 29, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FMS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL CABLE WAS BROKEN CAUSING THE SIDERAIL TO LOWER QUICKLY. 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 PEDIATRIC OPEN HOSPITAL BED FMS STRYKER MEDICAL FL19H NA

    Patients

    Seq Age Sex Outcome Treatment
    1