Draeger Medical recalls Atlan A350 anesthesia workstations with model 8211500 due to risk of piston ventilator failure before or during use. Affected units have specific serial numbers listed in the recall.
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 Medical is recalling Atlan A350 anesthesia workstations with model number 8211500 because they may indicate a failure of the piston ventilator before use or during actual ventilation. This could lead to inadequate anesthesia delivery to patients.
The Atlan anesthesia workstation may indicate a failure of the piston ventilator before use or suffer a failure of mechanical ventilation during use. This could result in inadequate anesthesia delivery to patients, potentially causing harm.
Healthcare professionals using Atlan A350 anesthesia workstations with model number 8211500 in the US are most at risk. Patients receiving anesthesia through these workstations could be affected.
Check if your Atlan A350 has model number 8211500. Affected units have specific serial numbers listed in the recall, including many starting with ASTB, ASTC, ASTD, ASTE, ASTF, ASTH, ASTJ, or ASTK prefixes.
Verify your Atlan A350 has model number 8211500. Affected units have specific serial numbers listed in the recall.
The model number is 8211500.
Affected units have specific serial numbers listed in the recall, including many starting with ASTB, ASTC, ASTD, ASTE, ASTF, ASTH, ASTJ, or ASTK prefixes.
The recall does not specify an immediate stop-use requirement. However, affected units may have a risk of ventilator failure, so it's recommended to check if your unit is affected.
We’ve drafted a message you can send Atlan to request your refund or repair — edit it as you like.
Subject: Recall Z-0304-2025 — Atlan Atlan Hello, I own a Atlan that is covered by recall Z-0304-2025 from Atlan. 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.
