BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PERIDOXRTU

    MDR report key: 24098477 · Received January 16, 2026

    Report

    Report Number
    MW5182369
    Event Type
    Malfunction
    Date Received
    January 16, 2026
    Date of Event
    January 9, 2026
    Report Date
    January 12, 2026
    Manufacturer
    CONTEC, INC.
    Product Code
    LRJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    WHEN A NEW BOTTLE OF PERIDOXRTU WAS OBTAINED FOR CLEANING IT WAS FOUND TO BE EXPANDED WITH GAS. THE PACKAGING WAS NOT OPENED AND PRODUCT NOT USED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    166321 PERIDOXRTU DISINFECTANT, MEDICAL DEVICES LRJ CONTEC, INC. GH090425251C

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown