Draeger Inc. recalls Atlan A350XL anesthesia workstations with serial numbers starting with ASTA-0307. The device may fail during ventilation use, causing potential harm to patients.
The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Draeger Inc. recalls Atlan A350XL anesthesia workstations that could fail during mechanical ventilation, potentially harming patients. This recall affects specific serial numbers sold in the U.S. and overseas.
The device may indicate a failure before use or suffer mechanical ventilation failure during use. This could lead to inadequate patient ventilation, risking patient harm during medical procedures.
Healthcare professionals using the Atlan A350XL anesthesia workstation for patient ventilation are most at risk. Patients undergoing surgery or diagnostic procedures with this device may be affected.
Check for serial numbers starting with ASTA-0307, ASTA-0309, ASTA-0311, ASTA-0349, or other listed codes in the U.S. and overseas. The device is an anesthesia workstation for adults, pediatrics, and neonates.
Look for the serial number on the device label, which starts with specific codes like ASTA-0307 or ASUB-0094.
Reach out to Draeger, Inc. for further assistance or to confirm if your device is affected.
The device may fail during ventilation use, so it is not safe to use without checking the recall status.
Check your device's serial number against the list provided in the recall notice to determine if it is affected.
Contact Draeger, Inc. directly for details about the recall and affected serial numbers.
We’ve drafted a message you can send Atlan to request your refund or repair — edit it as you like.
Subject: Recall Z-2617-2025 — Atlan Atlan Hello, I own a Atlan that is covered by recall Z-2617-2025 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.
