Draeger Medical recalls VentStar Basic 250 breathing circuits without water traps due to potential short circuits. These single-use sets risk incorrect connections and electrical issues. Affected units lack water traps for condensate collection.
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit
Draeger Medical is recalling VentStar Basic 250 breathing circuits that lack water traps. This design flaw can cause incorrect connections or short circuits, potentially leading to electrical issues during use.
The breathing circuits lack a water trap, which normally collects condensate. Without this component, improper connections can cause short circuits, potentially leading to electrical malfunctions during anesthesia procedures.
Healthcare providers using VentStar Basic 250 anesthesia machines with these breathing circuits are most at risk. Patients receiving anesthesia via these circuits could face electrical issues.
Check for VentStar Basic 250 anesthesia machines with breathing circuits labeled 'Catalog Number MP00350' that do not include a water trap. These circuits were sold without water traps for all lots.
Ensure the breathing circuit includes a water trap to prevent short circuits. If missing, stop using it immediately.
The breathing circuits lack a water trap, which can cause incorrect connections and short circuits during anesthesia procedures.
No, the circuits without water traps pose a risk of short circuits and incorrect connections, so they should not be used.
Look for VentStar Basic 250 breathing circuits with Catalog Number MP00350 that do not include 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-0737-2019 — Draeger Medical Draeger Medical Hello, I own a Draeger Medical that is covered by recall Z-0737-2019 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.
