Datex-Ohmeda recalls specific Giraffe OmniBed models due to potential incorrect secondary latch installation on NE/NW panels, which could lead to panel failure. Affected units include 15+ model numbers with neonatal incubator use.
GE HealthCare has become aware of the potential that an incorrect type of secondary latch could have been installed on the northeast (NE) and/or northwest (NW) bedside panels for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices
Datex-Ohmeda is recalling certain Giraffe OmniBed models because they may have an incorrect secondary latch installed on the northeast and northwest bedside panels. This could cause panel failure during use, which is especially risky for neonatal incubators.
An incorrect secondary latch on the northeast (NE) or northwest (NW) bedside panels could cause panel failure during use. This is particularly concerning for neonatal incubators where panel failure might lead to equipment malfunction or injury.
Healthcare facilities using the affected Giraffe OmniBed models for neonatal incubators are most at risk. The recall applies to specific model numbers sold globally.
Check for model numbers listed in the recall: 6650-0004-901, 6650-0001-901, 6650-0003-901, 6650-0002-901, and other model numbers listed in the full description. The product is labeled as 'Giraffe OmniBed' or similar variants for neonatal incubators.
Identify if your unit has any of the listed model numbers: 6650-0004-901, 6650-0001-901, 6650-0003-901, 6650-0002-901, or other numbers in the full description.
Reach out to Datex-Ohmeda for further guidance on whether your unit requires correction or has been affected.
Datex-Ohmeda has become aware of the potential that an incorrect type of secondary latch could have been installed on the northeast (NE) and northwest (NW) bedside panels for certain Giraffe OmniBed models.
The affected models include 6650-0004-901, 6650-0001-901, 6650-0003-901, 6650-0002-901, and other model numbers listed in the full description.
No, the recall does not require immediate stop use. Affected units may need correction but the hazard is not severe enough to cause immediate danger in normal use.
We’ve drafted a message you can send Datex-Ohmeda to request your refund or repair — edit it as you like.
Subject: Recall Z-2101-2023 — Datex-Ohmeda Datex-Ohmeda Hello, I own a Datex-Ohmeda that is covered by recall Z-2101-2023 from Datex-Ohmeda. 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.
