Draeger Inc. recalls VentStar Flex 220 breathing circuits (model MP00355) due to potential cracking. This could lead to breathing gas leaks during use. Affected units were sold starting in 2020.
The potential for cracks forming in the breathing circuit hose.
Draeger Inc. is recalling VentStar Flex 220 breathing circuits (model MP00355) because cracks may form in the breathing circuit hose. This could cause breathing gas leaks during use, potentially affecting patient safety.
Cracks in the breathing circuit hose could allow breathing gases to leak, potentially causing inadequate ventilation or gas exposure for patients. The breathing circuit is designed for single use only, so cracks may not be immediately noticeable.
Adult patients using VentStar Flex 220 breathing circuits for anesthesia. Healthcare providers who use these circuits are most at risk.
Check for the model number MP00355 on the breathing circuit. These units were sold starting in 2020 and are used with anesthesia machines for adult patients.
Inspect the breathing circuit hose for cracks or damage before use.
The product is designed for single use only. Cracks may form, so it's recommended to check for cracks before use.
Look for model number MP00355 on the breathing circuit. These units were sold starting in 2020.
Stop using the circuit immediately and contact Draeger Inc. for further instructions.
We’ve drafted a message you can send VentStar to request your refund or repair — edit it as you like.
Subject: Recall Z-1493-2025 — VentStar VentStar Hello, I own a VentStar that is covered by recall Z-1493-2025 from VentStar. 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.
