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Stellar 150Recalls & reported problems

Resmed Pty Ltd · Ventilator · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00619498241613), received between Mar 16, 2022 and Mar 16, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “No Display/Image” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • No Display/Image1

Patient problems

  • Low Oxygen Saturation1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 16, 2022No Display/Image

    BIPAP (RESMED STELLAR) STOPPED FUNCTIONING WITH NO APPRECIABLE PRESSURE BEING DELIVERED - SCREEN ALSO NOTED TO BE BLANK. RN ATTEMPTED TO TURN DEVICE BACK ON, HOWEVER, REPORTED TO KEEP TURNING OFF. PATIENT WITH DESATURATION TO SPO2 60'S AND PLACED BACK ON NASAL OXYGEN WITHOUT FURTHER INCIDENT AND IMPROVEMENT IN SATURATION. BIPAP MACHINE PULLED FROM SERVICE AND REPLACED WITH SUBSTITUTE MACHINE. PULLED MACHINE NOTED TO BE MARKEDLY WARM TO TOUCH.

    Patient problems: Low Oxygen Saturation

    MAUDE report 13782166 ↗

Other Ventilator, Continuous, Minimal Ventilatory Support,Facility Use devices

All Ventilator, Continuous, Minimal Ventilatory Support,Facility Use devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.