Quick Facts at a Glance
- Recall Date
- November 10, 2025
- Hazard Level
- HIGH
- Brand
- Draeger
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 10 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Draeger
- Product type
- Airway Connector
- Model numbers
- Model/Catalog Number: MP01840, UDI Number:04048675420736, Lot numbers: All lot numbers
- Sold at
- Multiple Retailers
- Where affected
- CA, FL, IL, NY, OH, OK, PA, SC +2 more
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
November 10, 2025
Reported by FDA DEVICE
December 17, 2025
RecallRadar source check
December 24, 2025
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
What You Should Do
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
About This Product
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.
Why This Is Dangerous
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.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients and healthcare providers face significant safety risks from using compromised equipment. Immediate action is necessary to prevent potential ventilation failures.
Practical Guidance
How to identify if yours is affected
- Check the model number on the airway connector: MP01840.
- Review any lot numbers associated with your device.
- Contact Draeger for confirmation if unsure about your product.
Where to find product info
The model number and UDI can typically be found printed on the device itself or on the packaging.
What timeline to expect
Expect a refund or replacement processing time of approximately 4-6 weeks once the return is initiated.
If the manufacturer is unresponsive
- Document your communication attempts with Draeger.
- Escalate the issue to the FDA if you receive no response.
- Consider contacting a medical device safety organization for further assistance.
How to prevent similar issues
- Always verify the recall status of medical devices before use.
- Ensure that all medical equipment is regularly inspected for cracks or defects.
- Stay informed about product safety alerts through reliable sources.
Documentation advice
Keep records of your purchase, including receipts, correspondence with Draeger, and any photos of the product showing its condition.
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Product Details
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.
Key Facts
- Recall date: November 10, 2025
- Quantity recalled: 14,420 units
- Affected states: CA, FL, IL, NY, OH, OK, PA, SC, TX, WI
- Global distribution includes multiple countries
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Safety Guide
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