GE Healthcare recalls Giraffe OmniBeds with Servo Oxygen modules due to potential oxygen level display inaccuracies. Affected units include specific incubators and warmers with listed serial numbers and part kits.
Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a different environmental oxygen level than what is displayed by the device, if a certain optional component referred to as the Servo Oxygen Module is installed.
GE Healthcare is recalling certain Giraffe OmniBeds that have the Servo Oxygen module installed because they might show incorrect oxygen levels. This could lead to unsafe oxygen levels for infants in the incubator or warmer.
The Servo Oxygen module can cause the device to display a different oxygen level than what is actually present. This might lead to unsafe oxygen levels for infants, but the hazard is not described as causing serious injury in normal use.
Parents or caregivers of infants using the recalled Giraffe OmniBed with the Servo Oxygen module. Infants in incubators or warmers are most at risk due to potential oxygen level inaccuracies.
Check if your Giraffe OmniBed has the Servo Oxygen module installed. Affected units include incubators with serial numbers HDHA through HDHQ and specific part kits like 6600-0233-850.
Verify if your device shows a different oxygen level than what is displayed on the screen.
Reach out to GE Healthcare for guidance on whether your unit is affected and next steps.
The Servo Oxygen module may cause the device to display an inaccurate oxygen level, which could lead to unsafe oxygen levels for infants.
Giraffe Incubators with serial numbers HDHA through HDHQ and specific part kits including 6600-0233-850.
No, the recall does not require immediate stop use; however, you should check if your device displays an inaccurate oxygen level.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2235-2020 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2235-2020 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.
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.
