Draeger recalled 191,470 units of the ErgoStar CM 45 airway connector on November 10, 2025. Users reported cracks in the hose of specific catheter mounts, posing a high risk to patients. The recall affects healthcare facilities worldwide, including multiple U.S. states.
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Draeger, Inc. or your healthcare provider for instructions. Notification method: Letter
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The ErgoStar CM 45 is an airway connector used in healthcare settings for mechanically ventilated patients. It conducts respiratory gases between the breathing system and the patient interface, such as an endotracheal tube.
Cracks in the hose of the connector can lead to improper ventilation, posing a serious risk to patient safety. This defect may result in inadequate delivery of respiratory gases.
This recall is not part of a broader industry pattern.
Patients relying on mechanical ventilation may face serious health risks due to potential device failure. Healthcare providers must ensure immediate discontinuation of use to prevent harm.
The model number and UDI can typically be found printed on the device packaging or on the device itself.
Expect refund processing to take approximately 4-6 weeks after the return is received.
Keep all correspondence from Draeger, as well as purchase receipts and records of any communication regarding the recall.
The recall includes the ErgoStar CM 45, Model/Catalog Number: MP01845. The product is used for conducting respiratory gases between the breathing system and the patient interface. It was distributed worldwide, including states such as California, Florida, and Texas.
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