BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    7141794

    MDR report key: 7141794 · Received December 22, 2017

    Report

    Report Number
    7141794
    Event Type
    Malfunction
    Date Received
    December 22, 2017
    Date of Event
    December 4, 2017
    Report Date
    December 8, 2017
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS NOTED THAT THE CATHETER TIP WAS FRAYED WHEN REMOVED FROM PACKAGING. DEVICE IS BRAUN INTROCAN SAFETY 24 G X3/4 INCH REF 4252500-02.

    Patients

    Seq Age Sex Outcome Treatment
    1 0 YR NO| NO OTHER THERAPIES