Draeger Recalls

8 recalls found for Draeger. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Draeger Vapor 3000 Anesthetic Vaporizer Recalled Due to Impurities

Draeger, Inc. recalled 188 units of the Vapor 3000 anesthetic vaporizer on November 24, 2025. The devices contained impurities in a component not delivered within specification. Healthcare providers and patients must stop using the devices immediately.

Draeger
A certain
Read more
Health & Personal Care
HIGH
FDA DEVICE

Draeger Vapor 2000 Anesthetic Vaporizer Recalled Over Impurities

Draeger, Inc. recalled 431 units of the Vapor 2000 anesthetic vaporizer on November 24, 2025. A component of the devices contained impurities and did not meet specifications, posing a high hazard risk. Healthcare providers and patients should cease use immediately and follow recall instructions.

Draeger
A certain
Read more
Health & Personal Care
HIGH
FDA DEVICE

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.

Draeger
Multiple complaints
Read more
Health & Personal Care
HIGH
FDA DEVICE

Draeger Recalls Airway Connector Over Cracking Hazard

Draeger recalled 118,850 airway connectors on November 10, 2025, due to cracking hazards. This recall affects multiple countries, including the United States and Australia. The device poses a serious risk to mechanically ventilated patients.

Draeger
Multiple complaints
Read more
Health & Personal Care
HIGH
FDA DEVICE

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.

Draeger
Multiple complaints
Read more
Health & Personal Care
HIGH
FDA DEVICE

Draeger Recalls Airway Connector Due to Cracking Hazard

Draeger recalled 2,050 units of the ErgoStar CM 60 airway connector on November 10, 2025. The recall follows multiple reports of cracks in the device, posing a risk to mechanically ventilated patients. Healthcare providers and patients should stop using the connector immediately.

Draeger
Multiple complaints
Read more
Health & Personal Care
HIGH
FDA DEVICE

Draeger Recalls Anesthesia Workstation After Ventilation Failures

Draeger recalled 223 Atlan A350XL anesthesia workstations on September 9, 2025. The devices may fail during mechanical ventilation, posing serious health risks. The recall affects states across the U.S. and several countries worldwide.

Draeger
The device
Read more

Brand Statistics

Total Recalls
8
Pages
1