Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction Recalled by Draeger, Inc. Due to Multiple complaints were reported in which cracks formed...

Date: November 10, 2025
Company: Draeger, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Draeger, Inc. directly.

Affected Products

ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.

Quantity: 14420 units

Why Was This Recalled?

Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.

Where Was This Sold?

This product was distributed to 10 states: CA, FL, IL, NY, OH, OK, PA, SC, TX, WI

Affected (10 states)Not affected

About Draeger, Inc.

Draeger, Inc. has 19 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report