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RecallWatchMedical Device Safety
Class IIOngoingZ-2475-2026

GE Medical Systems, LLC recalls Giraffe OmniBed

GE Medical Systems, LLCWaukesha, WI, United StatesReported Jun 24, 2026 · 24 days ago
Legal News Analyst ·

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.

Affected product

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Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models
    400 affected lots
    HDGP50034HDGP51018HDGS50069HDGS50070HDGS50074HDGS50077HDGS50158HDGS50162
    +392 moreHDGS52245HDGS52286HDGT50374HDGT50399HDGS50464HDGS50560HDGS50569HDGS50570HDGD50349HDGG54079HDGJ50278HDGJ50281HDGJ50390HDGJ50391HDGJ50394HDGJ50400HDGK52363HDGM50481HDGM50482HDGM50483HDGM50484HDGM50485HDGM50486HDGQ50625HDGQ50626HDGQ50627HDGQ50628HDGQ50629HDGS50369HDGS50370HDGS50371HDGS50372HDGR50086HDGL51597HDGG54268HDGG54270HDGG54410HDGK51696HDGL51002HDGL51003HDGL51004HDGL51005HDGL51032HDGN50383HDGP50522HDGQ50763HDGQ50882HDGQ50884HDGQ50886HDGQ50887HDGQ50901HDGQ50902HDGQ50903HDGQ50904HDGQ50905HDGQ50906HDGQ50907HDGQ50908HDGQ50909HDGQ50910HDGQ50911HDGQ50912HDGQ50913HDGQ50917HDGS51833HDGU60609HDGU60732HDGE50297HDGE50370HDGE50371HDGK51791HDGK51792HDGK51793HDGK51794HDGK51795HDGK51804HDGK51822HDGK51840HDGR50087HDGR50088HDGR50178HDGR50180HDGR50184HDGR50185HDGN50863HDGN50864HDGN50865HDGN50866HDGN50868HDGN50869HDGN50870HDGH60335HDGH60316HDGH60319HDGH60320HDGH60321HDGH60322HDGH60323HDGH60324HDGH60326HDGH60327HDGH60328HDGH60329HDGH60330HDGH60331HDGH60333HDGH60334HDGH60403HDGH60407HDGH60408HDGH60409HDGN50867HDGT50420HDGK51412HDGK51706HDGK52164HDGL50039HDGL51294HDGL51483HDGL51486HDGM51574HDGM51575HDGM51583HDGP51029HDGS52343HDGS52358HDGJ50055HDGN50393HDGM50726HDGM50093HDGM50146HDGM50149HDGM50151HDGP51237HDGP51290HDGP51297HDGQ51823HDGQ51947HDGJ51132HDGJ51133HDGJ51134HDGJ51136HDGJ51142HDGJ51176HDGJ51177HDGJ51180HDGJ51181HDGJ51182HDGJ51189HDGJ51190HDGL50080HDGL50082HDGL50123HDGL50165HDGR52333HDGS50800HDGS50812HDGU60084HDGU60087HDGU60098HDGU60157HDGU60158HDGU60162HDGU60168HDGU60598HDGT50753HDGT50754HDGT50756HDGT50757HDGU60516HDGU60520HDGU60523HDGU60527HDGU60528HDGU60533HDGU60535HDGU60540HDGU60542HDGU60543HDGJ51045HDGJ51079HDGQ50791HDGR52718HDGR52936HDGL51165HDGL51190HDGM51272HDGM51289HDGN51296HDGN51337HDGP50832HDGP50839HDGT50381HDGT50382HDGL51672HDGN51051HDGN51096HDGR50127HDGR50143HDGS50619HDGS50624HDGS50629HDGS50630HDGG55016HDGJ50424HDGJ50427HDGJ50432HDGK52226HDGM50995HDGM50996HDGM51000HDGM51003HDGM51005HDGM51009HDGQ50958HDGQ50961HDGQ50963HDGQ50965HDGQ50967HDGR52148HDGR52150HDGR52152HDGR52221HDGR52246HDGR52281HDGR52301HDGR52310HDGR52329HDGR52331HDGD00113HDGF50369HDGF53069HDGF53072HDGG55175HDGH60780HDGH60781HDGJ50183HDGJ50935HDGJ51027HDGK51849HDGM50511HDGQ51811HDGS50516HDGT60443HDGT60444HDGT60445HDGK52275HDGM50360HDGM50366HDGM50374HDGM50397HDGM50402HDGM50416HDGM50417HDGM50430HDGM50438HDGM50439HDGM50441HDGM50448HDGM50455HDGM50456HDGM50473HDGM50548HDGM50550HDGM50552HDGM50553HDGM50554HDGM50555HDGM50557HDGM50562HDGM50564HDGM50581HDGM50583HDGM50595HDGM50632HDGM50633HDGM50634HDGM50635HDGM50641HDGM50642HDGM50646HDGM50648HDGM50649HDGM50650HDGM50681HDGM50686HDGS52298HDGM50445HDGM50643HDGL50363HDGL51839HDGK51331HDGK51348HDGL51846HDGL51847HDGQ51109HDGQ51112HDGQ51116HDGQ51117HDGS50785HDGS50787HDGS52365HDGS52369HDGT60089HDGT60113HDGL50427HDGL50628HDGS50005HDGS50010HDGN50437HDGN50586HDGN50588HDGN50590HDGN50591HDGN50592HDGN50593HDGN50594HDGN50606HDGN50793HDGG54096HDGG54099HDGG54100HDGL51851HDGL51857HDGL51858HDGP50025HDGQ51891HDGT50691HDGM50788HDGM50789HDGN50790HDGH61006HDGS50355HDGS50755HDGH60898HDGE50352HDGJ50127HDGJ50133HDGJ50393HDGJ50396HDGJ50397HDGJ50399HDGJ50401HDGJ50404HDGJ50405HDGT50740HDGJ50654HDGJ50657HDGG54196HDGH60133HDGH60485HDGH60505HDGH60571HDGJ50175HDGK51252HDGK51350HDGS51933HDGS51974HDGS52066HDGS52088HDGS52149HDGS52151HDGK51230HDGK51232HDGK52080HDGK52081HDGK52189HDGK52190HDGK52194HDGK52195HDGK52263HDGN51268HDGN51306HDGN51308HDGJ51212HDGL51827HDGM51259HDGM51356HDGM51360HDGN50309HDGP50101HDGU60725HDGU60731HDGU60735HDGU60840HDGU60863HDGU60881HDGU63034HDGU63201HDGU63220HDGU63222HDGQ50008

What the firm is doing

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.

DistributionShow details

Worldwide - US Nationwide distribution.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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