BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PHOENIX INSTRUMENT

    MDR report key: 5725536 · Received June 13, 2016

    Report

    Report Number
    MW5062867
    Event Type
    Injury
    Date Received
    June 13, 2016
    Date of Event
    May 24, 2016
    Report Date
    May 25, 2016
    Manufacturer
    B-D
    Product Code
    JSG
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PHOENIX SYSTEM FOR IDENTIFICATION AND SENSITIVITY IN MICROBIOLOGY IS DOWN AND REQUIRED SERVICE CALL FROM MANUFACTURER TO FIX.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    374352 PHOENIX INSTRUMENT PHOENIX INSTRUMENT JSG B-D

    Patients

    Seq Age Sex Outcome Treatment
    1 19 YR Required Intervention