Draeger recalls specific models of unheated anesthetic vaporizers due to impure components that may affect calibration. Affected units include serial numbers starting with ASUK-1181 to ASUK-1620.
A certain component of affected devices was not delivered within specification and contained impurities.
Draeger is recalling certain models of their unheated anesthetic vaporizers because a component had impurities that could affect calibration. This means the device might not work properly, which could lead to incorrect anesthesia delivery during medical procedures.
The recalled devices contain a component that was not delivered within specification and had impurities. This could cause the vaporizer to be improperly calibrated, potentially leading to incorrect anesthesia dosing during medical procedures.
Medical professionals using the Draeger Vapor 3000 for anesthesia delivery are most at risk. Patients receiving anesthesia from these specific models could experience improper dosing.
Check for serial numbers starting with ASUK-1181 to ASUK-1620. The product is an unheated, calibrated anesthetic vaporizer manufactured by Draeger, Inc.
Look for the serial number on the device, which should start with ASUK-1181 to ASUK-1620.
The recall is due to a component that was not delivered within specification and contained impurities, which could affect calibration.
Check the serial number to see if it's in the affected range. If it is, contact Draeger for guidance.
The impure component could lead to improper calibration, potentially causing incorrect anesthesia dosing during medical procedures.
We’ve drafted a message you can send Draeger to request your refund or repair — edit it as you like.
Subject: Recall Z-0934-2026 — Draeger Draeger Hello, I own a Draeger that is covered by recall Z-0934-2026 from Draeger. 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.
