{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Madison",
      "address_1": "3030 Ohmeda Dr",
      "reason_for_recall": "Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a report for a bone density exam may be sent to PACS with the incorrect patient information in the DICOM header. The correct patient information will be listed on the DICOM report image; however, the report may appear under a different patients name in the PACS.",
      "address_2": "",
      "product_quantity": "43 units",
      "code_info": "a) DPX NT, Model Numbers: LU8230, LU40338, LU42357, LU42369  b) DPX MD+, Model Numbers:  LU8230, LU40338, LU40352",
      "center_classification_date": "20180417",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) including Puerto Rico and to the countries of : Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Egypt, Finland, France, Germany, Greece, Hong Kong, India, Ireland, Israel, Italy, Japan, Korea, Lebanon, Malaysia, Malta, Mexico, Morocco,  Norway, Poland, Portugal , Romania, Russia, Saudi Arabia, Spain, Switzerland, Taiwan, Tunisia, Turkey, United Arab, United Kingdom and Venezuela.",
      "state": "WI",
      "product_description": "GE Healthcare Lunar:   a) DPX NT, Model Numbers: LU8230, LU40338, LU42357, LU42369  b) DPX MD+, Model Numbers:  LU8230, LU40338, LU40352    Provides an estimate of BMD (Bone Marrow Density) at the lumbar spine and proximal femur regions. This BMD value can then be compared to a reference population at the sole discretion of the physician.",
      "report_date": "20180425",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Medical Systems Ultrasound & Primary Care Diagnostics, LL",
      "recall_number": "Z-1394-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79710",
      "termination_date": "20201214",
      "more_code_info": "",
      "recall_initiation_date": "20180316",
      "postal_code": "53718-6704",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}