{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Tustin",
      "address_1": "PO Box 2068",
      "reason_for_recall": "If two specific operations are performed in multi-phase helical scanning, the acquired raw data may not be saved.",
      "address_2": "2441 Michelle Dr",
      "product_quantity": "459",
      "code_info": "system software V6.0 or later",
      "center_classification_date": "20151009",
      "distribution_pattern": "US Distribution including Puerto Rico",
      "state": "CA",
      "product_description": "Toshiba Aquilion CT System  TSX-301A",
      "report_date": "20151021",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-0014-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
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      "termination_date": "20161026",
      "recall_initiation_date": "20150508",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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