Draeger recalls ID Circuit Flex 220 breathing circuits (model MP01347) due to potential cracks in the hose. Affected units may need replacement to prevent breathing gas leaks.
The potential for cracks forming in the breathing circuit hose.
Draeger is recalling ID Circuit Flex 2:220 breathing circuits (model MP01347) because cracks could form in the hose. This might cause breathing gas leaks, which could be dangerous if the circuit fails during use.
Cracks in the breathing circuit hose could allow breathing gases to leak. If the hose fails during use, this might cause inadequate gas delivery to the patient. However, the risk is low as the product is designed to prevent such issues.
Adults using the ID Circuit Flex 220 breathing circuit for anesthesia or ventilation. Those with the model number MP01347 are most at risk.
Check for the model number MP01347 on the breathing circuit. The product was sold with UDI number 04048675249337 and all lot numbers.
Inspect the breathing circuit hose for cracks or damage.
The recall states there is a potential for cracks forming in the hose, which could lead to breathing gas leaks. However, the risk is low as the product is designed to prevent such issues.
The recall does not specify a remedy, so you should check for cracks and contact Draeger if you find damage.
Look for the model number MP01347 on the breathing circuit. The product was sold with UDI number 04048675249337 and all lot numbers.
We’ve drafted a message you can send ID Circuit to request your refund or repair — edit it as you like.
Subject: Recall Z-1494-2025 — ID Circuit ID Circuit Hello, I own a ID Circuit that is covered by recall Z-1494-2025 from ID Circuit. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.