{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Torrance",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72683",
      "recalling_firm": "Shimadzu Medical Systems",
      "address_1": "20101 S Vermont Ave",
      "address_2": "N/A",
      "postal_code": "90502-1328",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution and Internationally to Canada",
      "recall_number": "Z-0451-2016",
      "product_description": "Mobile X-ray system MobileDaRt Evolution/FDR Go Software    The device is a mobile X-ray system and allows a technician to take a general digital radiography of patients in the hospital or medical facility who cannot move and outpatients in emergency.",
      "product_quantity": "297 units",
      "reason_for_recall": "The firm is recalling the Shimadzu Mobile X-ray system because an image may not transfer to image server properly.",
      "recall_initiation_date": "20151110",
      "center_classification_date": "20151218",
      "termination_date": "20161027",
      "report_date": "20151230",
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