BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BASIC NEURO ORTHO SPINE PK

    MDR report key: 14311811 · Received May 5, 2022

    Report

    Report Number
    MW5109566
    Event Type
    Malfunction
    Date Received
    May 5, 2022
    Date of Event
    April 30, 2022
    Report Date
    May 4, 2022
    Manufacturer
    PRESOURCE / CARDINAL HEALTH
    Product Code
    OJG
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    IMPROPER AMOUNT OF PRODUCT. FDA SAFETY REPORT ID# (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1839923 BASIC NEURO ORTHO SPINE PK NEUROLOGICAL TRAY OJG PRESOURCE / CARDINAL HEALTH 585398

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown