BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COMPRESSOR,NEBULIZER, CHARACTER, PUP

    MDR report key: 23496460 · Received November 7, 2025

    Report

    Report Number
    1417592-2025-00612
    Event Type
    Malfunction
    Date Received
    November 7, 2025
    Date of Event
    October 15, 2025
    Report Date
    November 7, 2025
    Manufacturer
    MEDLINE INDUSTRIES LP
    Product Code
    BTI
    UDI-DI
    00888277678166
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    IT WAS REPORTED THAT THE MACHINE IS NOT DISPENSING MEDICATION CORRECTLY LEADING TO MISSED MEDICATION. IN AN ABUNDANCE OF CAUTION, THIS MEDWATCH IS BEING FILED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTAINED, A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED.

    Description of Event or Problem · 0

    DEVICE NOT DISPENSING MEDICATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    172093 COMPRESSOR,NEBULIZER, CHARACTER, PUP BTI MEDLINE INDUSTRIES LP 6462308 00888277678166

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other