Recall
FDAHealthNovember 10, 2025

Draeger, Inc. — 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

⚠️ Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.

Is this relevant to me?

Geography
US, CA, FL, IL, NY, OH, OK, PA, SC, TX, WI
Source agency
FDA
Category
Health
Published
November 10, 2025

Worldwide distribution. US states of CA, FL, IL, NY, OH, OK, PA, SC, TX, and WI; Australia, Austria, Belarus, Belgium, Brazil, Bulgaria, Canada, Chile, China, Czech Republic, Ecuador, Finland, France, Germany, Hungary, Indonesia, Italy, Japan, Mexico, Netherlands, Norway, Pakistan, Poland, Portugal, Romania, Saudi Arabia, Serbia, Slovakia, South Africa, South Korea, Spain, Switzerland, Thailand, Turkiye, Ukraine, and United Kingdom.

What's affected?

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.
Lot code
All

Additional details

Model/Catalog Number: MP01840; UDI Number:04048675420736; Lot numbers: All lot numbers

What should I do?

Recommended action

Class I recall. Voluntary: Firm initiated Quantity affected: 14420 units.

View original FDA notice →

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