The Recall Desk

FDA (Devices) recall action 97923

Draeger, Inc. recalled 4 products on 2025-12-17

The FDA (Devices) publishes a recall like this one as 4 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 4 pages.

Products
4
Announced
2025-12-17
Critical
4
Units
326,790

Why these products were recalled

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

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

1–4 of 4

  • CriticalFDA (Devices)··2025-12-17

    Ventilator airway connectors recalled after cracks formed in the hose

    Draeger is recalling 191,470 ErgoStar CM 45 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.

    Product
    ErgoStar CM 45, Model/Catalog Number: MP01845, 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.
    Category
    Distribution
    10 states
  • CriticalFDA (Devices)··2025-12-17

    ErgoStar CM 60 airway connectors recalled after cracks formed in the hose

    Draeger is recalling 2,050 ErgoStar CM 60 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.

    Product
    ErgoStar CM 60, Model/Catalog Number: MP01860, 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.
    Category
    Distribution
    10 states
  • CriticalFDA (Devices)··2025-12-17

    ErgoStar CM 55 airway connectors recalled after cracks formed in the hose

    Draeger is recalling 118,850 ErgoStar CM 55 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.

    Product
    ErgoStar CM 55, Model/Catalog Number: MP01855, 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.
    Category
    Distribution
    10 states
  • CriticalFDA (Devices)··2025-12-17

    Frozen chikoo slices recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen chikoo slices after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    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.
    Category
    Distribution
    10 states