{
  "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": "2026-04-15",
    "results": {
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      "status": "Terminated",
      "city": "Torrance",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73745",
      "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": "Nationwide Distribution",
      "recall_number": "Z-1585-2016",
      "product_description": "X-Ray Diagnostic Table, Model No. YSF-300  Use in combination with an X-ray high voltage generator, an X-ray tube unit, an Image intensifier and X-ray television unit, this table is applied for the following X-ray examinations: -X-ray T.V. fluoroscopy -Spot-filming -Bucky radiography",
      "product_quantity": "185 units",
      "reason_for_recall": "Report of unintentional movement of table to reverse tilting.",
      "recall_initiation_date": "20160331",
      "center_classification_date": "20160428",
      "termination_date": "20170102",
      "report_date": "20160504",
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