BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 2072115 · Received April 21, 2011

    Report

    Report Number
    2072115
    Date Received
    April 21, 2011
    Date of Event
    April 1, 2011
    Report Date
    April 21, 2011
    Manufacturer
    B BRAUN
    Product Code
    FMI
    Report Source
    User Facility report
    Reporter Location
    DE, US

    Narratives

    Description of Event or Problem · 1

    NURSE INSERTED #22 SAFETY HUBER NEEDLE IN RIGHT PORT. FLUSHED WITH 20 ML OF NORMAL SALINE THAT INFILTRATED INTO CHEST. PULLED NEEDLE OUT AND IT WAS ALMOST COMPLETELY BENT TO THE SIDE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * HUBER NEEDLE FMI B BRAUN * WN60

    Patients

    Seq Age Sex Outcome Treatment
    1 *