Recall Z-2477-2026

GE Medical Systems, LLC · initiated May 1, 2026

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 6600-1461-500

Codes / lots: Serial Numbers: 5452896 801057486 800977619 801093759 5584569 5587625 5367527 5603110 5371240 5497382

Reason for recall

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

FDA-determined cause: Component design/selection

Action taken

An URGENT MEDICAL DEVICE CORRECTION notification letter dated 5/1/26 was sent to customers. Actions to be taken by Customer/User You may continue to use your device after performing the pre-use checkout in accordance with the Giraffe OmniBed Carestation User Manual (Chapter 6 Pre-Use Checkout). During the pre-use checkout described in the product User Manual, visually inspect the device for any damaged or missing components. This includes verifying that the canopy soffit is properly secured and that all six fasteners are present and fully engaged. If you observe damage, missing fasteners, or improper soffit attachment during the pre-use checkout, please remove the device from clinical use and contact GE HealthCare Service. Please ensure all potential users in your facility are made aware of this safety notification and the recommended actions. Please complete and return the attached acknowledgement form electronically via FMI 32101 Digital CRF or print, fill out manually, scan, and email to MIC.FMI32101@gehealthcare.com. Please retain this document for your records. Product Correction GE HealthCare will correct all affected products at no cost to you. A GE HealthCare representative will contact you to arrange for the correction. Contact Information If you have any questions or concerns regarding this notification, please contact GE HealthCare Service at 1-800-437-1171 or your local Service Representative. Please be assured that maintaining a high level of safety and quality is our highest priority. If you have any questions, please contact GE HealthCare per the contact information above.

Details

Recall number
Z-2477-2026
Initiated
May 1, 2026
Posted by FDA
June 17, 2026
Product code
FMZ – Incubator, Neonatal
Quantity
265 units
Distribution
Worldwide - US Nationwide distribution.
Recalling firm
GE Medical Systems, LLC, Waukesha, WI

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2475-2026 Class IIGiraffe OmniBed, a combination of an infant incubator and an infant warmer, All ModelsGE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel… 05/01/2026Open, Classified
Z-2476-2026 Class IIGiraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination of an…GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel… 05/01/2026Open, Classified