Reported Feb 12, 2014 · Terminated

Giraffe¿ Infant Warmers, part number M1118179, labeled in part *** GE Healthcare 8880 Gorman Road Laurel, MD…

GE Healthcare

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 Healthcare · 8880 Gorman Rd · Laurel, MD · 20723-5800

Is this the product you have?

  • Giraffe¿ Infant Warmers, part number M1118179, labeled in part *** GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com* Giraffe¿ Infant Warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology.
Lot codes and dates
  • Serial Numbers

    1,970 of 1,970 codes

    • HDJR52093
    • HDJQ52878
    • HDJS51010
    • HDJP51983
    • HDJN52273
    • HDJN52274
    • HDJN52275
    • HDJN52276
    • HDJP50604
    • HDJP50605
    • HDJM50388
    • HDJR56613
    • HDJQ52689
    • HDJR50734
    • HDJR50735
    • HDJS50028
    • HDJP52371
    • HDJP52558
    • HDJN51693
    • HDJN51694
    • HDJR56618
    • HDJQ51960
    • HDJS52390
    • HDJM50693
    • HDJM51714
    • HDJM51716
    • HDJM51717
    • HDJM51718
    • HDJM52096
    • HDJN52193
    • HDJN52194
    • HDJN52195
    • HDJN52196
    • HDJN52197
    • HDJP52562
    • HDJP52563
    • HDJP52564
    • HDJP52565
    • HDJQ52920
    • HDJQ52917
    • HDJQ52918
    • HDJQ52919
    • HDJQ52921
    • HDJQ52922
    • HDJQ52923
    • HDJQ52924
    • HDJQ52925
    • HDJQ52926
    • HDJQ52927
    • HDJQ53075
    • HDJR56481
    • HDJR56482
    • HDJR56486
    • HDJR56487
    • HDJR56488
    • HDJR56489
    • HDJR56490
    • HDJR56491
    • HDJR56358
    • HDJP50531
Amount recalled
1970 units

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Medical device adjustment knob may be loose and affect the accuracy of blended Air/Oxygen gas mixture to patients.

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.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 1, 2015 · Data as of Sep 19, 6:17 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.