BEUDAMED
    FDA Adverse Event Other Summary report: N

    BD L-CATH

    MDR report key: 478086 · Received August 12, 2003

    Report

    Report Number
    1710034-2003-00053
    Event Type
    Other
    Date Received
    August 12, 2003
    Report Date
    July 7, 2003
    Manufacturer
    BECTON DICKINSON INFUSION THERAPY SYSTEMS
    Product Code
    FOZ
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PICC WAS PLACED EASILY AND THEN THE STYLET WAS DIFFICULT TO REMOVE. THE CATHETER SEPARATED FROM THE HUB. THEY TRIMMED IT AND REPAIRED IT BUT THE CATHETER KEPT SHREDDING AS THEY TRIED TO FIX IT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD L-CATH PERCUTANEOUS CATHETER FOZ BECTON DICKINSON INFUSION THERAPY SYSTEMS NA 2302053

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other