Class 2 Medicines : Norgine Pharmaceuticals Limited, Pedmarqsi 80
OFFICIAL-SOURCE RECALL · UNITED KINGDOM
Dräger Atlan Anaesthesia workstations: ventilator failure Recall: In April 2026, Dräger issued a follow-up
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CountryUnited KingdomPublishedAugust 4, 2026Last updatedAugust 4, 2026Official source last checkedSeptember 9, 2026 at 1:48 PM UTC
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- Dräger Atlan Anaesthesia workstations: risk of ventilator failure (DSI/2026/005)
- Manufacturer
- See official notice
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
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.
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 failure.
What consumers should do
s are being completed. As of 29 July 2026, the manufacturer reports no confirmed patient injuries or deaths associated with this issue. Advice for Healthcare Professionals: identify whether your site uses Atlan Anaesthesia workstations and check if the devices are listed as affected in the FSN ensure Dräger replaces the motor assemblies in all your affected Atlan Anaesthesia workstations. Dräger will be in touch to arrange replacement of the motor assembly whilst waiting for Dräger to replace the motor assemblies, affected devices can continue to be used only with permanent supervision as per the instructions for use if mechanical ventilation fails, use manual/ spontaneous ventilation mode to ventilate the patient as needed if the error occurs during use, the mechanical ventilation may fail, and device alerts the user by displaying “Ventilator error!!!!”” with acoustic alarm. During ventilator failure the Atlan workstation will continue to provide: manual/spontaneous ventilation mode fresh gas and agent delivery all monitoring functions without restriction clinical staff should make sure they are familiar with the device’s manual ventilation mode, and local protocols for ventilatio
Official recall notice
Dräger Atlan Anaesthesia workstations: risk of ventilator failure (DSI/2026/005)
Agency: Medicines and Healthcare products Regulatory Agency
Official publication date: August 4, 2026
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