Draeger Medical recalls Set2Go Ventilation 12 (A) units due to risk of breathing circuit parts detaching during ventilation. All units are affected. Contact for remedy.
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 all Set2Go Ventilation 12 (A) units because glued connections in the breathing circuit can become loose, potentially causing parts to detach during use. This could lead to partial or complete detachment of pieces, which may affect ventilation safety.
The breathing circuit connections are glued together but can become loose over time. This may cause pieces to detach during ventilation, potentially disrupting the device's function and posing a risk to patient safety.
Healthcare professionals using the Set2Go Ventilation 12 (A) device are most at risk, as loose parts could interfere with ventilation during medical procedures.
Check for the Set2Go Ventilation 12 (A) model with UDI-DI: 04048675544739. All units are affected, regardless of when they were purchased.
Verify if your Set2Go Ventilation 12 (A) has the UDI-DI: 04048675544739 identifier.
Reach out to Draeger Medical for specific instructions on remedy or replacement.
Yes, all Set2Go Ventilation 12 (A) units with UDI-DI: 04048675544739 are affected.
Contact Draeger Medical for specific instructions on remedy or replacement.
The recall does not specify a fix, so it is recommended to 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-1459-2023 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-1459-2023 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.
