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TheBrief.Health

Living with device recall

Stories from people navigating device recall — diagnosis, treatment, caregiving, and the ordinary days in between.

2 stories

A Luna G3 positive airway pressure device being checked against a recall notice in a sleep clinic.

Innovation & Devices

Luna G3 APAP Recall: Identifying Patients at Risk

An FDA Class I recall covers Luna G3 APAP model LG3600 with specified firmware. Clinicians and suppliers need to identify exposed patients and protect continuity of positive airway pressure therapy.

Rayan Salih · September 25, 2026 · 6 min

An Astral ventilator beside checked backup equipment and a device inventory label in a respiratory care setting.

Innovation & Devices

Astral Ventilator Recall and Supercapacitor Failure Risk

Certain ResMed Astral 100 and 150 ventilators require correction because supercapacitor leakage may contribute to failure. Ventilator-dependent patients need prompt device checks and reliable backup plans.

Rayan Salih · 6 min read

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