RecallRadar

FDA Device recall Z-3080-2024

GE Giraffe Warmer, Model/Catalog Number M1118179-01090979

On 2024-10-02 the FDA classified a Class II recall of GE Giraffe Warmer, Model/Catalog Number M1118179-01090979 by Wipro Ge Healthcare Private, citing 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 electri….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-3080-2024
ClassificationClass II
Statusongoing
Initiated2024-08-09
Published2024-10-02
Last updated2026-09-13 11:57 UTC
CompanyWipro Ge Healthcare Private
Distributionn/a

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.

Identifiers

code_infoSerial Number GBW24230381SA

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3080-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.