---
title: "GE Heathcare Giraffe OmniBed Carestation, Model Number 2082844-001-XXX; neo n... — FDA record Z-0048-2025 | Is It on Recall"
description: "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"
url: https://isitonrecall.com/recall/fda-device-z-0048-2025-ge-heathcare-giraffe-omnibed-carestation-model-number-2082844-001-xxx-neo-natal-incubator/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# GE Heathcare Giraffe OmniBed Carestation, Model Number 2082844-001-XXX; neo natal incubator — FDA record Z-0048-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 3, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: GE Heathcare Giraffe OmniBed Carestation, Model Number 2082844-001-XXX; neo natal incubator
- **Reason**: 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.
- **Classification**: Class I
- **Recalling firm**: DATEX--OHMEDA, INC.
- **Quantity**: Not supplied
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0048-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0048-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | All models |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Oct 23, 2024
- **Recall initiation date**: Sep 3, 2024
- **Center classification date**: Oct 17, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0048-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [DATEX--OHMEDA, INC. records](https://isitonrecall.com/brand/datex-ohmeda-inc/)