Draeger Medical recalls VentStar Anesthesia 180 models due to risk of breathing circuit detachment during use. Affected units have specific serial numbers and were sold in the U.S. Learn how to check and what to do.
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Draeger Medical is recalling VentStar Anesthesia 180 anesthesia machines because glued connections in the breathing circuit can become loose, potentially causing parts to detach during use. This could lead to breathing problems for patients if not fixed.
The breathing circuit's glued connections can become loose before or during ventilation. This may cause partial or complete detachment of circuit pieces, which could interfere with the patient's breathing.
Healthcare providers using VentStar Anesthesia 180 machines in hospitals or clinics are most at risk. Patients receiving anesthesia through these machines could be affected if the circuit detaches.
Check the product label for the model number 'VentStar Anesthesia (N) 180' and serial number starting with '04048675422198'. All units produced are affected.
Look for the model number 'VentStar Anesthesia (N) 180' and serial number starting with '04048675422198' to confirm if your unit is affected.
This recall affects VentStar Anesthesia 180 machines with serial numbers starting with 04048675422198. Check your label to see if you're affected.
The recall record does not specify a remedy, so contact Draeger Medical directly for guidance on next steps.
The hazard description states that loose connections could cause partial or complete detachment of circuit pieces, which might interfere with breathing. However, the recall does not specify a risk of serious injury in normal use.
We’ve drafted a message you can send Draeger Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1447-2023 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-1447-2023 from Draeger Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
