“Draeger ErgoStar CM 60 Airway Connector Recall: Hose Cracks Risk Injury.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/50696-draeger-ergostar-cm-60-airway-connector-recall-hose-cracks-risk. Based on FDA recall #Z-0593-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0593-2026%22&limit=1).
The FDA announced on Nov. 10, 2025, that Draeger, Inc. is recalling ErgoStar CM 60 airway connectors due to cracks in the hose. The agency classified the recall as Class I and ongoing.
How to tell if you have it
Brand: Draeger
Product: ErgoStar CM 60 Airway connector
Model/Catalog Number: MP01860
UDI Number: 04048675420699
Lot numbers: All lot numbers
Quantity: 2050 units
The hazard
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts. The product is an airway connector for conduction of respiratory gases between the breathing system and the patient interface.
Context
GovInfoNow's records show Draeger, Inc. has issued six other recalls since March 12, 2025. Recent brand recalls include a Sept. 3, 2026 recall of VentStar Resus Neo units for potential hose cracks and a May 7, 2026 recall of the Atlan A350 Anesthesia Workstation for ventilator failure risk. Other recent recalls of similar products include B. Braun Medical Spinal Epidural Pump Model 530184 (Jan. 29, 2026), B. Braun Medical NES1725KFXL Spinal Epidural Catheter (Jan. 29, 2026), and B. Braun Medical CESK Harris Methodist (Jan. 29, 2026).
How to tell if you have this one
Check for the model number MP01860 on the connector. The product was sold with lot numbers covering all production batches.
Brand
Draeger
Category
Medical device
FDA recall event · 4 products
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Ongoing
Distribution
Worldwide distribution. US states of CA, FL, IL, NY, OH, OK, PA, SC, TX, and WI; Australia, Austria, Belarus, Belgium, Brazil, Bulgaria, Canada, Chile, China, Czech Republic, Ecuador, Finland, France, Germany, Hungary, Indonesia, Italy, Japan, Mexico, Netherlands, Norway, Pakistan, Poland, Portugal, Romania, Saudi Arabia, Serbia, Slovakia, South Africa, South Korea, Spain, Switzerland, Thailand, Turkiye, Ukraine, and United Kingdom.
Recall number
Product, codes & lots
Quantity
Z-0590-2026
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.; Model/Catalog Number: MP01840; UDI Number:04048675420736; Lot numbers: All lot numbers
14420 units
Z-0591-2026
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.; Model/Catalog Number: MP01845; UDI Number: 04048675420729; Lot numbers: All lot numbers;
191470 units
Z-0592-2026
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.; Model/Catalog Number: MP01855; UDI Number: 04048675420705; Lot numbers: All lot numbers;
118850 units
Z-0593-2026
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.; Model/Catalog Number: MP01860; UDI Number: 04048675420699; Lot numbers: All lot numbers;
2050 units
Based on the official FDA remedy
What to do — step by step
Check for Cracks
Inspect the hose for cracks or damage before use.
Where it went and when
Where it was distributed
Distributed in 10 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “Worldwide distribution. US states of CA, FL, IL, NY, OH, OK, PA, SC, TX, and WI; Australia, Austria, Belarus, Belgium, Brazil, Bulgaria, Canada, Chile, China, Czech Republic, Ecuador, Finland, France, Germany, Hungary, Indonesia, Italy,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Florida, Illinois, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Texas, Wisconsin.
Recall timeline
FDA published this recall 37 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0593-2026 (November 10, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0593-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.