ResMed Ltd. recalls
7 recalls in our records from 2015 to 2026: 7 FDA medical devices.
Recalls with full detail pages
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ResMed Ltd. medical device recall: Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system…
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation…
Earlier and other recalls
These link to the official agency notice.
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ResMed Ltd. medical device recall: AirFit N10 Nasal Masks and User Guide Official notice ↗
Masks non-invasive interface for channeling airflow to patients have magnets that have potential magnetic interference with active medical implants that interact with…
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ResMed Ltd. medical device recall: Astral 100 and Astral 150 ventilators Official notice ↗
If ventilator is on internal battery, not intended to serve as a primary power source, low/critically low battery alarms will sound, but a fault leads to sudden power…
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ResMed Ltd. medical device recall: ResMed Stellar Official notice ↗
Combination of software and a component failure may cause audible alarms not to operate properly, the alarm buzzer not work, for ventilators that have a failed…
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Resmed Corporation medical device recall: Quattro Air FFM MED AMER Official notice ↗
Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size Medium actually contain a non-vented (NV) Quattro Air FFM Large mask.
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Resmed Corporation medical device recall: Astral 100 Official notice ↗
Resmed Corporation is recalling Astral 100, 150 External Battery because of a start-up issue.
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ResMed Ltd. medical device recall: Astral 100 Official notice ↗
The Astral device allows clinicians to disable all alarms including those that detect circuit disconnection. Inappropriate disabling of alarms in ventilator dependent…
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.