🔍 RecallPedia

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.

Class I - Dangerous
🏥 Medical Devices Recalled: November 10, 2025 Draeger Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Model/Catalog Number: MP01840; UDI Number:04048675420736; Lot numbers: All lot numbers
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Draeger, Inc.
Reason for Recall:
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

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.

Product Codes/Lot Numbers:

Model/Catalog Number: MP01840; UDI Number:04048675420736; Lot numbers: All lot numbers

Distribution:

Distributed in: US, CA, FL, IL, NY, OH, OK, PA, SC, TX, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0590-2026

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