{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "86338",
      "product_res_number": "Z-0600-2010",
      "event_date_initiated": "2009-02-01",
      "event_date_posted": "2010-01-27",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-12-31",
      "res_event_number": "53692",
      "product_code": "KGI",
      "product_description": "iDXA, GE Lunar DEXA bone densitometers operating with enCORE software versions 12.0, 12.1, 12.2,13.0, & 13.1.  \n\nThe systems provide an estimate of BMD",
      "code_info": "software versions 12.0, 12.1, 12.2,13.0, & 13.1.",
      "firm_fei_number": "3005860720",
      "recalling_firm": "Ge Healthcare",
      "address_1": "9900 W Innovation Dr",
      "city": "Wauwatosa",
      "state": "WI",
      "postal_code": "53226-4856",
      "reason_for_recall": "Failure to properly pre-indicate the technique factors to be used during a patient scan.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "An Important Electronic Product Radiation Warning letter will be sent to customers.  The letter will discuss the defect description and related hazards, the affected product details, safety instructions, and product correction.  Customers are to contact their local GE Healthcare service representative with questions.",
      "product_quantity": "1,764 total",
      "distribution_pattern": "Nationwide Distribution",
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        "medical_specialty_description": "Radiology",
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}