BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RELIZORB

    MDR report key: 25233423 · Received May 20, 2026

    Report

    Report Number
    MW5188494
    Event Type
    Injury
    Date Received
    May 20, 2026
    Date of Event
    March 30, 2026
    Report Date
    May 18, 2026
    Manufacturer
    UNK
    Product Code
    PLQ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PATIENT WAS HOSPITALIZED FROM MARCH 30-APRIL 1 DUE TO A RENAL VIRUS. THEY ARE STILL USING RELIZORB.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    348057 RELIZORB ENZYME PACKED CARTRIDGE PLQ UNK 3430790000

    Patients

    Seq Age Sex Outcome Treatment
    1 3 YR Female Hospitalization