{
  "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": "2026-05-06",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath",
      "address_2": "",
      "product_quantity": "3,796 units",
      "code_info": "All serial numbers",
      "center_classification_date": "20120608",
      "distribution_pattern": "Worldwide Distribution.",
      "state": "WI",
      "product_description": "GE Healthcare Definium 8000 Digital Radiographic Systems :   GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188  Model Number: 5131070.    The Revolution XR/d with Tomosynthesis is intended for use in generating Tomographic images of human anatomy. It is not intended for mammographic use.",
      "report_date": "20120620",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "General Electric Med Systems LLC",
      "recall_number": "Z-1789-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "37654",
      "termination_date": "20120731",
      "more_code_info": "",
      "recall_initiation_date": "20060531",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}