Home/Recalls/UK-MHRA-drager-atlan-anaesthesia-workstations-risk-of-ventilator-failure-dsi-slash-2026-slash-005
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Dräger Atlan Anaesthesia workstations: risk of ventilator failure (DSI/2026/005)

Published: August 4, 2026Recall ID: drager-atlan-anaesthesia-workstations-risk-of-ventilator-failure-dsi-slash-2026-slash-005Category: devicesCountry: UK
UK
Medical DeviceUKUK

Dräger Atlan Anaesthesia workstations: risk of ventilator failure (DSI/2026/005)

Recalling Firm: MHRA

Reason for Recall / Hazard

In April 2026, Dräger issued a follow-up Field Safety Notice expanding the number of Atlan Anaesthesia workstation devices affected by a manufacturing defect that may result in mechanical ventilation ...

Product Description & Identification

In April 2026, Dräger issued a follow-up Field Safety Notice expanding the number of Atlan Anaesthesia workstation devices affected by a manufacturing defect that may result in mechanical ventilation failure.

Affected Products

Dräger Atlan Anaesthesia workstations: risk of ventilator failure (DSI/2026/005)

Additional Source Details

FieldValue
Guidtag:www.gov.uk,2005:/drug-device-alerts/drager-atlan-anaesthesia-workstations-risk-of-ventilator-failure-dsi-slash-2026-slash-005
Linkhttps://www.gov.uk/drug-device-alerts/drager-atlan-anaesthesia-workstations-risk-of-ventilator-failure-dsi-slash-2026-slash-005
Pub Date2026-08-04T14:00:13+01:00
Extracted categorydevices

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Overview

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