ErgoStar CM 40 Model/Catalog Number: MP01840 Airway co... (Draeger, Inc.) – multiple complaints were reported in ... (2025)
Catheter mount cracks can potentially compromise respiratory gas conduction.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
Brand
Draeger, Inc.
Lot Codes / Batch Numbers
Model/Catalog Number: MP01840, UDI Number:04048675420736, Lot numbers: All lot numbers
Products Sold
Model/Catalog Number: MP01840; UDI Number:04048675420736; Lot numbers: All lot numbers
Draeger, Inc. is recalling ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction of respiratory gases due to Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Recommended Action
Per FDA guidance
On November 10, 2025, Urgent Medical Device Recall letters were sent to customers. Necessary Action: Identify if you have any affected product. Do not use any unused ErgoStar CM 40/CM 45/CM 55/CM 60 in your stock. Unused stock should be removed and returned to Draeger. Draeger recommends the alternative product MP01850 ErgoStar CM 50 as a suitable replacement. Please ensure that all potential users in your facility are made aware of this Urgent Medical Device Recall Notice and the information contained herein. If you have forwarded affected products to third parties, please also forward this Urgent Medical Device Recall notification.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, IL, NY, OH, OK, PA, SC, TX, WI
Page updated: Jan 10, 2026