Reported Jun 24, 2026 · Ongoing

Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination of an infant incubator and an infant…

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 Carestations and Giraffe OmniBed Carestation CS1, a combination of an infant incubator and an infant warmer, Model Numbers 2082844-001-XXX
Lot codes and dates
  • UDI-DI010084068211686221
  • Serial Numbers

    2,794 of 2,794 codes

    • TAB24430068SA
    • TAB24430069SA
    • TAB24430070SA
    • TAB24430071SA
    • TAB26011006SA
    • TAB26011009SA
    • TAB26021001SA
    • TAB26061022SA
    • TABW63370
    • TAB24300033SA
    • TABV60214
    • TABW63378
    • TAB24240010SA
    • TABV62327
    • TABA70043
    • TABA70053
    • TABA70054
    • TABA70055
    • TABZ72515
    • TABV60081
    • TABV60219
    • TABV60221
    • TABV60223
    • TABV60224
    • TAB25351023SA
    • TAB25501502SA
    • TAB25501503SA
    • TAB25501530SA
    • TAB25501531SA
    • TAB26021501SA
    • TAB26021503SA
    • TAB26101502SA
    • TAB26101503SA
    • TAB26101507SA
    • TAB26101509SA
    • TAB26101510SA
    • TAB26101511SA
    • TAB26101512SA
    • TAB26101513SA
    • TAB26101515SA
    • TAB26101516SA
    • TAB26101517SA
    • TAB26101519SA
    • TAB26101520SA
    • TAB26101521SA
    • TABX63854
    • TABX63855
    • TABX63856
    • TAB25111019SA
    • TAB24160010SA
    • TABY70926
    • TABY70987
    • TABX63393
    • TAB24280002SA
    • TABV60007
    • TABV60203
    • TABW63326
    • TABX62677
    • TABX62757
    • TABX63717
    TABX
Amount recalled
23430 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.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new GE Medical Systems, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:55 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.