BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RELIZORB

    MDR report key: 24701304 · Received March 26, 2026

    Report

    Report Number
    MW5185939
    Event Type
    Injury
    Date Received
    March 26, 2026
    Report Date
    March 20, 2026
    Manufacturer
    ALCRESTA THERAPEUTICS, INC.
    Product Code
    PLQ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    RELIZORB CARTRIDGE KEEPS BREAKING. THE COMPANY IS AWARE OF THE FAULTY PLASTIC BUT WILL NOT REPLACE OUR SUPPLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    756344 RELIZORB ENZYME PACKED CARTRIDGE PLQ ALCRESTA THERAPEUTICS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention