{
  "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": "2026-08-20",
    "results": {
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      "cfres_id": "45051",
      "product_res_number": "Z-0757-06",
      "event_date_initiated": "2006-03-27",
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      "recall_status": "Terminated",
      "event_date_terminated": "2012-03-13",
      "res_event_number": "34975",
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      "firm_fei_number": "1418957",
      "recalling_firm": "Fischer Imaging Corporation",
      "address_1": "12300 North Grant Street",
      "city": "Denver",
      "state": "CO",
      "postal_code": "80241-3120",
      "additional_info_contact": "303-254-2585",
      "reason_for_recall": "Software upgrade to preclude lost images during mammography procedure.",
      "root_cause_description": "Other",
      "action": "Consignees were notified by letter on 03/27/2006.",
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        "device_name": "Full Field Digital, System, X-Ray, Mammographic",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1715",
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}