Home/Recalls/UK-MHRA-national-patient-safety-alert-resmed-astral-100-and-150-ventilators-potential-for-patient-harm-due-to-unexpected-interruption-of-ventilation-therapy-natpsa-slash-2026-slash-004-slash-mhra
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National Patient Safety Alert: ResMed Astral 100 and 150 Ventilators: Potential for Patient Harm due to Unexpected Interruption of Ventilation Therapy (NatPSA/2026/004/MHRA)

Published: August 17, 2026Recall ID: national-patient-safety-alert-resmed-astral-100-and-150-ventilators-potential-for-patient-harm-due-to-unexpected-interruption-of-ventilation-therapy-natpsa-slash-2026-slash-004-slash-mhraCategory: devicesCountry: UK
UK
Medical DeviceUKUK

National Patient Safety Alert: ResMed Astral 100 and 150 Ventilators: Potential for Patient Harm due to Unexpected Interruption of Ventilation Therapy (NatPSA/2026/004/MHRA)

Recalling Firm: MHRA

Reason for Recall / Hazard

ResMed has issued a Field Safety Notice regarding Astral 100 and 150 ventilators and associated Printed Circuit Board Assembly spare parts manufactured prior to October 2024. A fault in the device can...

Product Description & Identification

ResMed has issued a Field Safety Notice regarding Astral 100 and 150 ventilators and associated Printed Circuit Board Assembly spare parts manufactured prior to October 2024. A fault in the device can cause unexpected interr…

Affected Products

National Patient Safety Alert: ResMed Astral 100 and 150 Ventilators: Potential for Patient Harm due to Unexpected Interruption of Ventilation Therapy (NatPSA/2026/004/MHRA)

Additional Source Details

FieldValue
Guidtag:www.gov.uk,2005:/drug-device-alerts/national-patient-safety-alert-resmed-astral-100-and-150-ventilators-potential-for-patient-harm-due-to-unexpected-interruption-of-ventilation-therapy-natpsa-slash-2026-slash-004-slash-mhra
Linkhttps://www.gov.uk/drug-device-alerts/national-patient-safety-alert-resmed-astral-100-and-150-ventilators-potential-for-patient-harm-due-to-unexpected-interruption-of-ventilation-therapy-natpsa-slash-2026-slash-004-slash-mhra
Pub Date2026-08-17T09:30:35+01:00
Extracted categorydevices

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Overview

  • Recalling FirmMHRA
  • Risk LevelMedical Device Alert
  • DistributionUnited Kingdom
Recall Hazard Severity
Caution (Class III)
Official Agency Alert

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