BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RELIZORB 500 ML MILLILITRE(S)

    MDR report key: 10349638 · Received July 30, 2020

    Report

    Report Number
    MW5095813
    Event Type
    Injury
    Date Received
    July 30, 2020
    Report Date
    July 28, 2020
    Manufacturer
    ALCRESTA THERAPEUTICS, INC.
    Product Code
    PLQ
    UDI-DI
    62205000020
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT IS IN THE HOSPITAL AT THIS TIME FOR GI.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    808252 RELIZORB 500 ML MILLILITRE(S) ENZYME PACKED CARTRIDGE PLQ ALCRESTA THERAPEUTICS, INC. 3330200000 62205000020

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization