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: MP01845, UDI Number: 04048675420729, 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 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.
Why This Is Dangerous
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.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
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.
Practical Guidance
How to identify if yours is affected
- Check if the model number is MP01845.
- Look for any visible cracks in the hose of the connector.
- Verify if the product was received from a healthcare provider.
Where to find product info
The model number and UDI can typically be found printed on the device packaging or on the device itself.
What timeline to expect
Expect refund processing to take approximately 4-6 weeks after the return is received.
If the manufacturer is unresponsive
- Document your communication attempts with Draeger.
- Reach out to your healthcare provider for assistance.
- Consider contacting consumer protection agencies if necessary.
How to prevent similar issues
- Always check for recall notices before using medical devices.
- Look for safety certifications on medical equipment.
- Ensure devices are maintained and inspected regularly.
Documentation advice
Keep all correspondence from Draeger, as well as purchase receipts and records of any communication regarding the recall.
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Product Details
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.
Key Facts
- Recall date: November 10, 2025
- Quantity recalled: 191,470 units
- Hazard level: High
- Affected model: MP01845
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Safety Guide
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