BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIFEGLOBAL® MEDIA

    MDR report key: 18815759 · Received March 1, 2024

    Report

    Report Number
    18815759
    Event Type
    Malfunction
    Date Received
    March 1, 2024
    Date of Event
    November 27, 2023
    Report Date
    November 29, 2023
    Manufacturer
    LIFEGLOBAL GROUP, LLC
    Product Code
    MQL
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    IA
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    CULTURE MEDIA DEFINITELY DID NOT SUPPORT EMBRYO DEVELOPMENT TO THE BLASTOCYST STAGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    296858 LIFEGLOBAL® MEDIA MEDIA, REPRODUCTIVE MQL LIFEGLOBAL GROUP, LLC LGGG-050 231020-018742

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown