GE Healthcare recalls Avance CS2 and Aisys CS2 anesthesia systems with a crack risk in the base that could cause falls. Affected units have specific serial numbers and GTINs. Contact GE Healthcare for details.
The base of the anesthesia system can have a crack and could potentially fracture resulting in a tip or overbalance of the anesthesia system. This can result in potential injury if it falls on a person.
GE Healthcare is recalling certain anesthesia systems because the base can crack, potentially causing the system to tip over and fall on a person. This could lead to injury if the device falls during use.
The base of the anesthesia system can develop a crack, which may cause the system to become unstable. If the system tips over, it could fall on a person, leading to potential injury.
Healthcare providers using the recalled anesthesia systems are most at risk. Patients receiving anesthesia through these systems could be affected if the device falls.
Check for the specific serial numbers or GTINs listed: Avance CS2 and Avance CS2 Pro have GTIN 00840682102322, while Aisys CS2 has GTIN 00840682102292. The product names and part numbers are also listed in the recall notice.
Look for the serial number on the device or its packaging to confirm if it's affected.
Reach out to GE Healthcare for further instructions on how to address the issue.
The base of the anesthesia system can crack, potentially causing the system to tip over and fall on a person, which could lead to injury.
Check the serial number or GTIN listed in the recall notice: Avance CS2 and Avance CS2 Pro have GTIN 00840682102322, while Aisys CS2 has GTIN 00840682102292.
Contact GE Healthcare for further instructions on how to address the issue.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1427-2022 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-1427-2022 from GE Healthcare. 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.
