BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD BONANNO CATHETER

    MDR report key: 493867 · Received November 4, 2003

    Report

    Report Number
    2618282-2003-00006
    Event Type
    Injury
    Date Received
    November 4, 2003
    Date of Event
    March 28, 2003
    Report Date
    November 4, 2003
    Manufacturer
    BECTON DICKINSON CARIBE LTD
    Product Code
    FEZ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    BONANNO SUPRAPUBIC BLADDER DRAINAGE CATHETER WAS USED AS A CHEST DRAIN. THE CATHETER WAS INSERTED ON THE WARD IN 3/2003 INTO THE CHEST OF THE PT. TWO WEEKS LATER A NURSE REMOVED THE SUTURES AND THE CATHETER CAME AWAY ALMOST IMMEDIATELY, LEAVING 14-15CMS OF IT WITHIN THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD BONANNO CATHETER BONANNO SUPRAPUBIC BLADDER DRAINAGE CATHETER FEZ BECTON DICKINSON CARIBE LTD NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention