BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CUG PEDIATRIC CRIB - FIXE BASE

    MDR report key: 2933426 · Received December 21, 2012

    Report

    Report Number
    1831750-2012-13170
    Event Type
    Malfunction
    Date Received
    December 21, 2012
    Date of Event
    November 28, 2012
    Report Date
    November 28, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FMS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    ASSIST CABLE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE RIGHT SIDE RAIL COULD DROP UNINTENTIONALLY DUE TO A BROKEN ASSIST CABLE. THE CUSTOMER REPORTED THAT THEY DID NOT KNOW IF THERE WAS ANY PT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CUG PEDIATRIC CRIB - FIXE BASE PEDIATRIC OPEN HOSPITAL BED FMS STRYKER MEDICAL FL19F NA

    Patients

    Seq Age Sex Outcome Treatment
    1