Draeger Medical recalls Seattle PAP Plus devices with model MP02260 sold before March 20, 2023. Glued breathing circuit connections can become loose, causing partial or complete detachment of pieces during ventilation.
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 Seattle PAP Plus devices with model MP02260 that were sold before March 20, 2023. Glued connections in the breathing circuit can become loose during ventilation, potentially causing pieces to detach and block airflow.
The breathing circuit has glued connections that can become loose before or during ventilation. This may cause partial or complete detachment of pieces, blocking airflow and potentially causing breathing difficulties.
People using the Seattle PAP Plus device for medical ventilation are affected. Those with breathing difficulties or medical conditions requiring continuous ventilation are at higher risk.
Check for the model number MP02260 on the device. Devices sold before March 20, 2023 (lots other than 0367.2702.13) are affected.
Look for the model number MP02260 on the device.
Contact Draeger Medical for specific instructions on how to handle the device.
The breathing circuit connections can become loose during ventilation, potentially causing pieces to detach and block airflow. This may affect users requiring continuous ventilation.
Check for the model number MP02260 and ensure it was sold before March 20, 2023 (lots other than 0367.2702.13).
Contact Draeger Medical for specific instructions on how to handle the device.
We’ve drafted a message you can send Draeger Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1439-2023 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-1439-2023 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.
