Draeger Medical recalls VentStar Watertrap 18:00 (P) 180 breathing circuits without water traps due to potential incorrect connections causing short circuits. All units are affected.
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit
Draeger Medical is recalling VentStar Watertrap (P) 180 breathing circuits that lack a water trap. This can lead to incorrect connections or short circuits in the breathing circuit, which may cause breathing issues during medical procedures.
The breathing circuit is incorrectly assembled without a water trap, which can cause improper connections. This may lead to short circuits in the breathing circuit, potentially disrupting the flow of respiratory gases during medical procedures.
Healthcare providers using anesthesia machines or ventilators with these breathing circuits are most at risk. Patients receiving anesthesia through these circuits could face breathing complications.
Check for the VentStar Watertrap (P) 180 model with Catalog Number MP00361. These breathing circuits are intended for single use only and lack a water trap.
Ensure the breathing circuit includes a water trap as part of the assembly. If missing, it is part of the recalled product.
The breathing circuit is incorrectly assembled without a water trap, which can cause incorrect connections or short circuits in the breathing circuit.
Check for the VentStar Watertrap (P) 180 model with Catalog Number MP00361. These breathing circuits are intended for single use only and lack a water trap.
Ensure the breathing circuit includes a water trap as part of the assembly. If missing, it is part of the recalled product.
We’ve drafted a message you can send Draeger Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0740-2019 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-0740-2019 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.
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.
