Draeger Medical recalls ID Circuit Basic 250 breathing circuits without water traps due to potential short circuits from incorrect assembly. These single-use anesthesia sets may cause electrical issues during medical procedures.
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit
Draeger Medical is recalling breathing circuits for anesthesia machines that lack water traps. The issue could cause short circuits if improperly assembled, potentially disrupting medical procedures.
The breathing circuits lack water traps, which are necessary for proper assembly. Without water traps, the circuits may short circuit when incorrectly connected, causing electrical issues during anesthesia delivery.
Healthcare providers using anesthesia machines with these specific breathing circuits are most at risk. Patients receiving anesthesia through these circuits could face electrical issues during procedures.
Check for the ID Circuit Basic 250 model with Catalog Number MP01348. These breathing circuits are sold without water traps and are intended for single use only.
Verify if your breathing circuit has the ID Circuit Basic 250 model with Catalog Number MP01348.
Reach out to Draeger Medical for guidance on whether your circuit needs replacement.
The breathing circuits lack water traps, which can cause short circuits if incorrectly assembled during medical procedures.
Yes, incorrect assembly could cause electrical issues during anesthesia delivery, potentially disrupting procedures.
Look for the ID Circuit Basic 250 model with Catalog Number MP01348, which is sold without water traps.
We’ve drafted a message you can send Draeger Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0743-2019 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-0743-2019 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.
