---
title: "GE Giraffe Warmer, Model/Catalog Number M1118179-01090979. Infant radiant war... — FDA record Z-3080-2024 | Is It on Recall"
description: "GE HealthCare has become aware that complete electrical safety testing was not conducted during manufacturing of certain Giraffe and Panda iRes Warmers. There a"
url: https://isitonrecall.com/recall/fda-device-z-3080-2024-ge-giraffe-warmer-model-catalog-number-m1118179-01090979-infant-radiant-warmers-provide-infrared-hea/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# GE Giraffe Warmer, Model/Catalog Number M1118179-01090979. Infant radiant warmers provide infrared heat in a controll... — FDA record Z-3080-2024

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 Aug 9, 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 Giraffe Warmer, Model/Catalog Number M1118179-01090979. Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Infant radiant warmers may be used to facilitate the neonate's transition to the external environment or to provide a controlled open environment.
- **Reason**: GE HealthCare has become aware that complete electrical safety testing was not conducted during manufacturing of certain Giraffe and Panda iRes Warmers. There are multiple electrical safety protections included in the product design. However, because the electrical safety testing in manufacturing was incomplete for these devices, there is the potential for leakage current to exceed IEC 60601 limits.
- **Classification**: Class II
- **Recalling firm**: Wipro GE Healthcare Private Ltd.
- **Quantity**: 1
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-3080-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3080-2024%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 | Serial Number GBW24230381SA |

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

## Distribution

US and Australia, Denmark, France, Germany, Ireland, ITALY, New Zealand, Poland, Portugal, Slovenia, Spain, SWITZERLAND, United Arab Emirates, United Kingdom.

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

## Dates in the source

- **Report date**: Oct 2, 2024
- **Recall initiation date**: Aug 9, 2024
- **Center classification date**: Sep 20, 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-3080-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Wipro GE Healthcare Private Ltd. records](https://isitonrecall.com/brand/wipro-ge-healthcare-private-ltd/)