Draeger Medical recalls ID Circuit Basic 180 breathing circuits without water traps due to potential short circuits. These single-use anesthesia sets may cause incorrect connections or electrical issues during use.
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit
Dra: Draeger Medical is recalling ID Circuit Basic 180 breathing circuits (Catalog Number MP01350) that lack a water trap. This design flaw could cause incorrect connections or short circuits, potentially leading to electrical issues during anesthesia procedures.
The breathing circuits lack a water trap, which is necessary for preventing electrical short circuits. Without this component, improper connections could cause the circuit to short, potentially leading to electrical issues during anesthesia procedures.
Healthcare providers using anesthesia machines or ventilators with these breathing circuits are most at risk. Patients receiving anesthesia through these circuits could face electrical hazards.
Check for the ID Circuit Basic 180 model with Catalog Number MP01350. These breathing circuits are sold without a water trap and are intended for single use only.
Ensure the breathing circuit includes a water trap; if missing, it is part of the recalled product.
The breathing circuits lack a water trap, which can cause incorrect connections or short circuits during anesthesia procedures.
The recall does not provide a fix; the remedy is not stated in the official notice.
Look for the ID Circuit Basic 180 model with Catalog Number MP01350, which is sold without a water trap.
We’ve drafted a message you can send Draeger Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0744-2019 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-0744-2019 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.
