BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CUB PEDIATRIC CRIB-HYD BASE

    MDR report key: 2933425 · Received December 21, 2012

    Report

    Report Number
    1831750-2012-13177
    Event Type
    Malfunction
    Date Received
    December 21, 2012
    Date of Event
    December 4, 2012
    Report Date
    December 4, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FMS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    WHEELS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THERE WAS REDUCED BRAKING FORCE DUE TO THE CASTERS COMING APART ON THE WHEELS. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CUB PEDIATRIC CRIB-HYD BASE CLOSED PEDIATRIC HOSPITAL BED FMS STRYKER MEDICAL FL19H NA

    Patients

    Seq Age Sex Outcome Treatment
    1