Draeger recalls Atlan A300 anesthesia workstations with model 8211300 due to potential piston ventilator failure before use or mechanical ventilation failure during use. Affected units have specific serial numbers.
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 A300 anesthesia workstations with model number 8211300 because they may fail the piston ventilator before use or mechanical ventilation during use. This could lead to serious medical risks for patients during anesthesia procedures.
The anesthesia workstation may fail its piston ventilator before use or experience mechanical ventilation failure during use. This could lead to inadequate breathing support for patients during anesthesia, potentially causing serious medical complications.
Healthcare professionals using the Atlan A300 anesthesia workstation for adult, pediatric, or neonatal patients are most at risk. The affected units have specific serial numbers listed in the recall.
Check for the model number 8211300 on the Atlan A300 anesthesia workstation. Affected units have specific serial numbers listed in the recall notice, including those starting with ASTA, ASTB, ASTC, ASTD, ASTE, ASTF, ASTH, or ASTK prefixes.
Review the serial numbers on your Atlan A300 anesthesia workstation to see if they match the list of affected serial numbers provided in the recall.
The model number for the recalled Atlan A300 is 8211300.
Affected serial numbers start with ASTA, ASTB, ASTC, ASTD, ASTE, ASTF, ASTH, or ASTK prefixes and include specific numbers listed in the recall notice.
The recall does not require immediate stop use; however, you should check if your unit is affected before continuing use.
We’ve drafted a message you can send Draeger to request your refund or repair — edit it as you like.
Subject: Recall Z-0667-2025 — Draeger Draeger Hello, I own a Draeger that is covered by recall Z-0667-2025 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.
