Official recall record

GE Heathcare Giraffe OmniBed; neo natal incubator

US FDA — Medical Devices · 2024-09-03 · United StatesClass I

Issuing authority: US FDA — Medical Devices
Alert date: 2024-09-03
Country of alert: United States
Alert level: Class I
Alert type: recall
Brand on record: DATEX--OHMEDA, INC.

What the authority reported

GE HealthCare has become aware that for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices, the screw that secures the doors that cover the warmer heaters may not have been torqued to specification. This may lead to the doors becoming loose.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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