BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DREAMSTATION BIPAP ST30

    MDR report key: 18415445 · Received December 28, 2023

    Report

    Report Number
    2518422-2023-38339
    Event Type
    Malfunction
    Date Received
    December 28, 2023
    Date of Event
    November 23, 2023
    Manufacturer
    RESPIRONICS, INC.
    Product Code
    MNS
    PMA / PMN Number
    K102465
    Removal / Correction Number
    Z-1972-2021
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    DEVICE EVALUATED BY THIRD PARTY.

    Additional Manufacturer Narrative · 0

    THE MANUFACTURER RECEIVED INFORMATION IN RELATION TO A DREAMSTATION BIPAP ST30 H/HT UNIT. THE DEVICE WAS RETURNED TO A THIRD PARTY SERVICE CENTER. DURING VISUAL INSPECTION OF THE DEVICE, IT WAS DETERMINED THE POWER CONNECTOR OF THE UNIT WAS CORRODED. DEVICE WAS SCRAPPED AT CUSTOMER'S REQUEST. ANALYSIS OF PAST EVENTS HAS NOT INDICATED AN ADVERSE EVENT HAS OCCURRED DUE TO CORROSION. REVIEW OF THE RISK FILE INDICATES THE POTENTIAL FOR A SERIOUS ADVERSE EVENT OCCURRING AS A RESULT OF THIS INCIDENT IS UNLIKELY. ADDITIONALLY, THE RISK FILE INDICATES THAT CORROSION WILL NOT SUBSTANTIALLY AFFECT THE PERFORMANCE OF THE DEVICE. THIS COMPLAINT IS CONSIDERED NOT REPORTABLE.

    Description of Event or Problem · 0

    THE MANUFACTURER RECEIVED INFORMATION REGARDING A DREAMSTATION BIPAP DEVICE. THE DEVICE WAS RETURNED TO A THIRD-PARTY SERVICE CENTER. DURING VISUAL INSPECTION OF THE DEVICE, IT WAS FOUND THAT THE POWER WAS CORRODED. THIS REPORT IS BEING SUBMITTED FOR POWER CORROSION FOUND DURING SERVICE. THERE WAS NO ALLEGATION OF SERIOUS OR PERMANENT HARM OR INJURY. NO MEDICAL INTERVENTION WAS REQUIRED FOR THE PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1489582 DREAMSTATION BIPAP ST30 VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING MNS RESPIRONICS, INC. DSX1030T11

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown