Draegerwerk recalls Atlan A350 gas machines (catalog 8621500/8621600) due to risk of unexpected shutdown from battery failure during use without AC power.
Internal backup battery may fail spontaneously while the Atlan is being operated without AC mains supply, resulting in unexpected shutdown of the device while running on batteries.
Draegerwerk is recalling Atlan A350 gas machines that may shut down unexpectedly while running on battery power. This could disrupt medical treatment during anesthesia or pain management procedures.
The internal backup battery can fail spontaneously when the machine is running on battery power without AC power. This may cause the device to shut down unexpectedly during medical procedures, potentially interrupting treatment.
Healthcare professionals using the Atlan A350 gas machine for anesthesia or analgesia are most at risk. Patients receiving treatment with these devices may be affected if the machine shuts down unexpectedly.
Check for catalog numbers 8621500 (Atlan A350) or 8621600 (Atlan A350 XL) on the device. The product was sold with specific lot numbers listed in the recall notice.
Verify if the machine is operating on battery power without AC connection, as this may trigger the hazard.
Reach out to Draegerwerk for guidance on whether the device needs repair or replacement.
This recall applies to specific Atlan A350 gas machines with catalog numbers 8621500 or 8621600. Check your device's catalog number to see if it's affected.
The recall does not specify immediate action for unexpected shutdowns. Contact Draegerwerk for assistance if this occurs.
Look for catalog numbers 8621500 (Atlan A350) or 8621600 (Atlan A350 XL) on the device. The recall includes specific lot numbers listed in the notice.
We’ve drafted a message you can send Draegerwerk to request your refund or repair — edit it as you like.
Subject: Recall Z-0971-2024 — Draegerwerk Draegerwerk Hello, I own a Draegerwerk that is covered by recall Z-0971-2024 from Draegerwerk. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
