Draeger Medical recalls VentStar Basic 180 breathing circuits without water traps due to potential short circuits. These single-use sets may cause incorrect connections or electrical issues during anesthesia.
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit
Dra: Draeger Medical is recalling VentStar Basic 180 breathing circuits (Catalog Number MP00349) that lack a water trap. This design flaw could cause short circuits or incorrect connections during anesthesia use, potentially leading to safety risks.
The breathing circuits lack a water trap, which can cause condensation buildup. This may lead to incorrect electrical connections or short circuits during use, potentially disrupting anesthesia delivery.
Healthcare professionals using VentStar Basic 180 anesthesia machines with these breathing circuits are most at risk. Patients receiving anesthesia through these circuits could face electrical issues.
Check for the VentStar Basic 180 model with Catalog Number MP00349. These breathing circuits do not have a water trap and are intended for single use only.
Ensure the breathing circuit has a water trap to avoid short circuits.
The breathing circuits lack a water trap, which can cause condensation buildup and lead to short circuits during anesthesia use.
No, these circuits without water traps have a risk of short circuits and incorrect connections, so they should not be used.
The recall record does not specify a remedy, so contact Draeger Medical for guidance.
We’ve drafted a message you can send Draeger Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0736-2019 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-0736-2019 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.
