Draeger Medical recalls Anesthesia Circuit Kit Coax 3 (MP02732) due to glued connections that may become loose, causing partial or complete detachment during ventilation. All units are affected.
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 its Anesthesia Circuit Kit Coax 3 (MP027:32) because glued connections can become loose, potentially causing parts to detach during ventilation. This could lead to breathing issues for patients under anesthesia.
The glued connections in the breathing circuit can loosen before or during ventilation. This may cause pieces to partially or completely detach, interrupting the patient's breathing circuit and risking breathing problems.
Healthcare professionals using the Anesthesia Circuit Kit Coax 3 for patient anesthesia are most at risk. Patients receiving anesthesia with this kit could experience breathing complications.
Check for the product name 'Anesthesia Circuit Kit Coax 3' with model number MP02732. All units are affected, regardless of lot number.
Identify the model number MP02732 on the product label to confirm if it's affected.
The recall states that glued connections can become loose, potentially causing detachment during ventilation. Using the product without checking for the recall may pose a risk.
Look for the model number MP02732 on the Anesthesia Circuit Kit Coax 3 product label. All units are affected.
The recall does not specify a remedy, so contact Draeger Medical directly 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-1453-2023 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-1453-2023 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.
