Draeger Medical recalls ID Circuit Watertrap 18:00 (P) 180 breathing circuits without water traps due to potential short circuits. All units are affected.
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit
Draeger Medical recalls breathing circuits without water traps that could cause short circuits. This risk affects anesthesia equipment used during medical procedures.
The breathing circuit lacks a water trap, which can lead to incorrect connections and short circuits. This may disrupt the anesthesia delivery system during medical procedures.
Healthcare providers using anesthesia machines or ventilators with these breathing circuits. Patients receiving anesthesia are at risk if the circuit malfunctions.
Check for the ID Circuit Watertrap (P) 180 model with Catalog Number MP01341. These breathing circuits are sold without water traps and are intended for single use only.
Ensure the breathing circuit includes a water trap; if not, it is affected.
The breathing circuit lacks a water trap, which can cause incorrect connections and short circuits.
Yes, all lots of the ID Circuit Watertrap (P) 180 with Catalog Number MP01341 are affected.
Check if the breathing circuit has a water trap; if not, it is affected and should be checked for short circuits.
We’ve drafted a message you can send Draeger Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0742-2019 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-0742-2019 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.
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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.
