BEUDAMED
    FDA Adverse Event Summary report: N

    B. BRAUN

    MDR report key: 2973810 · Received February 15, 2013

    Report

    Report Number
    MW5029019
    Date Received
    February 15, 2013
    Date of Event
    February 13, 2013
    Report Date
    February 15, 2013
    Manufacturer
    B. BRAUN
    Product Code
    FOZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    A RN STARTED IV WITH THIS PRODUCT - 22 GAUGE INTROCAN SAFETY BY B. BRAUN. UPON CLEANING UP HE REPORTED HE WAS STUCK ON FINGER BY EXPOSED NEEDLE TIP BECAUSE HE SAYS THE NEEDLE WAS RETRACTED THROUGH THE LOCKED POSITION. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    69375 B. BRAUN INTROCAN SAFETY 22 GX 1" PU FOZ B. BRAUN 4251628-02 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR