Data Foundry

Medical device recalls 2024

GE Giraffe Warmer — Class II medical device recall Z-3080-2024

Ongoing recall by Wipro GE Healthcare Private Ltd., reported 2024-10-02. GE HealthCare has become aware that complete electrical safety testing was not conducted during manufacturing

Recall numberZ-3080-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmWipro GE Healthcare Private Ltd., Bengaluru, India
Recall initiated2024-08-09
Classified2024-09-20
Reported by FDA2024-10-02
Countries outside the USAE, AU, CH, DE, DK, ES, FR, GB, IE, IT, NZ, PL, PT, SI
Quantity1
Reason classespackaging
Serial numbersGBW24230381SA
Model numbersM1118179-01090979

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 for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3080-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.