Reported Jun 24, 2026 · Ongoing

Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models

GE Medical Systems, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Medical Systems, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models
Lot codes and dates
  • Serial Numbers

    3,258 of 3,258 codes

    • HDGP50034
    • HDGP51018
    • HDGS50069
    • HDGS50070
    • HDGS50074
    • HDGS50077
    • HDGS50158
    • HDGS50162
    • HDGS52245
    • HDGS52286
    • HDGT50374
    • HDGT50399
    • HDGS50464
    • HDGS50560
    • HDGS50569
    • HDGS50570
    • HDGD50349
    • HDGG54079
    • HDGJ50278
    • HDGJ50281
    • HDGJ50390
    • HDGJ50391
    • HDGJ50394
    • HDGJ50400
    • HDGK52363
    • HDGM50481
    • HDGM50482
    • HDGM50483
    • HDGM50484
    • HDGM50485
    • HDGM50486
    • HDGQ50625
    • HDGQ50626
    • HDGQ50627
    • HDGQ50628
    • HDGQ50629
    • HDGS50369
    • HDGS50370
    • HDGS50371
    • HDGS50372
    • HDGR50086
    • HDGL51597
    • HDGG54268
    • HDGG54270
    • HDGG54410
    • HDGK51696
    • HDGL51002
    • HDGL51003
    • HDGL51004
    • HDGL51005
    • HDGL51032
    • HDGN50383
    • HDGP50522
    • HDGQ50763
    • HDGQ50882
    • HDGQ50884
    • HDGQ50886
    • HDGQ50887
    • HDGQ50901
    • HDGQ50902
    HDGR
Amount recalled
19587 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.