Draeger Medical recalls VentStar Anesthesia WT (P)180 models due to risk of breathing circuit detachment during use. Affected units may require repair or replacement to prevent injury.
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 Anesthesia WT (P)180 anesthesia machines 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 machine is used improperly.
The breathing circuit's glued connections can become loose before or during ventilation, causing partial or complete detachment of parts. This could lead to breathing issues if the machine is used improperly.
Anesthesia machine users, particularly healthcare professionals and patients undergoing surgery. Those using the VentStar Anesthesia WT (P)180 model are most at risk.
Check for the model number 'VentStar Anesthesia WT (P)180' on the device. All units produced with the serial number starting with 04048675421948 are affected.
Inspect the breathing circuit for loose connections that could detach during ventilation.
Reach out to Draeger Medical for guidance on repairs or replacements.
This recall affects VentStar Anesthesia WT (P)180 models with the serial number starting with 04048675421948. Check your device's serial number to confirm.
Draeger Medical does not provide specific repair instructions in this recall notice. Contact them directly for assistance.
No immediate stop is required, but you should check for loose connections and contact Draeger Medical for guidance.
We’ve drafted a message you can send Draeger Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1444-2023 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-1444-2023 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.
