HIGH

Draeger Recalls Airway Connector Over Cracking Hazard

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.

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

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

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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.

The Hazard

Cracks in the hose of specific catheter mounts can compromise the device's function. This poses a significant risk to mechanically ventilated patients.

Reported Incidents

Multiple complaints reported cracks in the connectors. No specific injury or death counts are provided.

What to Do

Stop using the device immediately. Follow the manufacturer's instructions for returning the product.

Contact Information

Contact Draeger, Inc. for further instructions at [insert specific contact number]. More information is available at the FDA's recall page.

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 Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Brand
Model Numbers
Model/Catalog Number: MP01840
UDI Number:04048675420736
Lot numbers: All lot numbers
Affected States
CA, FL, IL, NY, OH, OK, PA, SC, TX, WI
Report Date
December 17, 2025
Source Agency
FDA - Medical Devices
Recall Status
ACTIVE

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