Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models
FDA Recall Z-2475-2026 · Posted 2026-06-17
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Recalling FirmGE Medical Systems, LLC
Recall StatusOpen, Classified
Product CodeFMZ
Date Initiated2026-05-01
Product Quantity19587 units
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.
Firm Action
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 [email protected].
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.
Root Cause
Component design/selection
Distribution Pattern
Worldwide - US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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