Draeger Medical recalls VentStar Watertrap 180 models due to risk of breathing circuit parts detaching during ventilation. Affected units have specific serial numbers and were sold from 2013 onward.
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Dra: Draeger Medical is recalling VentStar Watertrap 180 models because glued connections in the breathing circuit can become loose, potentially causing parts to detach during ventilation. This could lead to breathing issues if the device is used improperly.
The breathing circuit's glued connections can become loose before or during ventilation. This may cause partial or complete detachment of parts, which could interfere with the device's function and pose a risk to the user's breathing.
Healthcare professionals using VentStar Watertrap 180 devices for ventilation are most at risk. Patients using these devices could also be affected if the breathing circuit detaches.
Check for the model number 'VentStar Watertrap (P) 180' and serial number starting with 04048675422013. All units produced since 2013 are affected.
Look for the serial number starting with 04048675422013 on the device.
Reach out to Draeger Medical for further guidance on the recall.
The product is not safe to use as the breathing circuit connections can become loose, potentially causing parts to detach during ventilation.
Check for the model number 'VentStar Watertrap (P) 180' and serial number starting with 04048675422013.
Contact Draeger Medical for further guidance on the recall.
We’ve drafted a message you can send Draeger Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1442-2023 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-1442-2023 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.
