Draeger recalls Atlan A350 anesthesia workstations with model 8211500 due to potential piston ventilator failure before use or mechanical ventilation failure during use. Affected units have specific serial numbers listed in the recall notice.
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Draeger is recalling Atlan A350 anesthesia workstations with model number 8211500 because they may fail during use, causing serious harm to patients. This recall affects healthcare facilities that use these workstations for anesthesia procedures.
The anesthesia workstation may indicate a failure of the piston ventilator before use or suffer a mechanical ventilation failure during use. This could lead to inadequate oxygen delivery or other serious complications for patients under anesthesia.
Healthcare facilities using the Atlan A350 anesthesia workstation with model number 8211500 are most at risk. Patients receiving anesthesia could be harmed if the workstation fails during surgery.
Check if your anesthesia workstation has model number 8211500. Affected units include specific serial numbers listed in the recall notice, such as ASSL-0347, ASSL-0348, and others.
Verify your anesthesia workstation has model number 8211500.
Reach out to Draeger for further instructions on the recall.
The model number is 8211500.
Affected serial numbers include ASSL-0347, ASSL-0348, ASSL-0351, and others as listed in the recall notice.
Check if your workstation has model number 8211500 and one of the specific serial numbers listed in the recall notice.
We’ve drafted a message you can send Draeger to request your refund or repair — edit it as you like.
Subject: Recall Z-2207-2026 — Draeger Draeger Hello, I own a Draeger that is covered by recall Z-2207-2026 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.
