Draeger recalled 14,420 units of its ErgoStar CM 40 airway connector on November 10, 2025, due to cracks forming in the hose. The recall affects multiple states in the U.S. and several countries worldwide.
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 40 Airway Connector is used in healthcare settings to facilitate the conduction of respiratory gases between the breathing system and the patient interface. It is critical for mechanically ventilated patients, making its reliability essential.
Cracks in the airway connector can lead to improper ventilation, endangering patient safety. Such defects can result in insufficient oxygen delivery, posing a serious risk during critical care.
This recall is not part of a broader industry pattern.
Patients and healthcare providers face significant safety risks from using compromised equipment. Immediate action is necessary to prevent potential ventilation failures.
The model number and UDI can typically be found printed on the device itself or on the packaging.
Expect a refund or replacement processing time of approximately 4-6 weeks once the return is initiated.
Keep records of your purchase, including receipts, correspondence with Draeger, and any photos of the product showing its condition.
The recalled product is the ErgoStar CM 40 Airway Connector, Model/Catalog Number: MP01840. It was distributed globally, including the U.S. states of CA, FL, IL, NY, OH, OK, PA, SC, TX, and WI.
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