HIGH

Draeger Recalls Airway Connector Due to Cracks in Hose

Draeger recalled 191,470 units of the ErgoStar CM 45 airway connector on November 10, 2025. Users reported cracks in the hose of specific catheter mounts, posing a high risk to patients. The recall affects healthcare facilities worldwide, including multiple U.S. states.

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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

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.

The Hazard

Reports indicate that cracks formed in the hose of specific catheter mounts, which could compromise patient ventilation. This defect poses a significant risk for mechanically ventilated patients.

Reported Incidents

There are multiple complaints regarding the cracked hoses, but specific injury or incident counts have not been disclosed. No deaths have been reported.

What to Do

Stop using the airway connector immediately. Follow the recall instructions provided by Draeger and contact your healthcare provider for further guidance.

Contact Information

For assistance, contact Draeger, Inc. at the number provided in your recall letter or visit their website for more details.

Key Facts

  • Recall date: November 10, 2025
  • Quantity recalled: 191,470 units
  • Hazard level: High
  • Distribution: Worldwide
  • Affected model: MP01845

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

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

Product Classification

Product Details

Brand
Model Numbers
Model/Catalog Number: MP01845
UDI Number: 04048675420729
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

Related Recalls

HIGH

Novo Nordisk Recalls Wegovy Injection Due to Contamination Risk

Novo Nordisk recalled Wegovy (semaglutide) Injection on December 19, 2025, due to hair found in a prefilled syringe. The recall affects products distributed nationwide in the United States. Consumers should stop using the product immediately and contact their healthcare provider.

Wegovy
Presence of
Read more
HIGH

Zydus Pharmaceuticals Recalls TraZODONE Tablets Over Defects

Zydus Pharmaceuticals recalled over 2,100 bottles of TraZODONE Hydrochloride Tablets on December 19, 2025. Some tablets have surface dents that may affect medication integrity. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Zydus Pharmaceuticals
Failed Tablet/Capsule
Read more
HIGH

Merck Recalls Noxafil Oral Suspension Due to Metal Contamination

Merck Sharp & Dohme LLC recalled 845 kits of Noxafil Powdermix on December 12, 2025. The recall follows the discovery of potential metal particulates in the product. Consumers should stop using the medication immediately and contact their healthcare provider for further guidance.

NOXAFIL
Presence of
Read more
HIGH

Merck Emend Recalled Due to Potential Metal Contamination

Merck Sharp & Dohme LLC recalled 3 single-dose kits of Emend (aprepitant) on December 12, 2025. The recall stems from the potential presence of metal particulates in the medication. Consumers should immediately stop using the product and contact their healthcare provider for guidance.

EMEND
Presence of
Read more
HIGH

Beaver-Visitec Recalls Laser and Endoscopy System Over Safety Hazard

Beaver-Visitec International recalled five units of the OME6000U Laser and Endoscopy System on December 5, 2025. The recall stems from a manufacturing deviation where ferrites required for the USB cable were not installed. This omission poses a high electrical hazard risk to patients and healthcare providers.

Beaver-Visitec International
Manufacturing deviation
Read more