{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tustin",
      "address_1": "2441 Michelle Dr",
      "reason_for_recall": "Scanning may be interrupted due to an error during execution of the eXam Plan and the system is unable to be shut down normally, resulting in the need to forcibly turn the system power off and reboot.  Loss of the acquired raw data would occur.",
      "address_2": "",
      "product_quantity": "10 devices",
      "code_info": "Canon Aquilion PRIME, TSX-303A - Serial numbers 1CB1892050, FLC1882279, FLC1892282, FLC1882278, FLC18Y2301, FLC1892288, FOC1892284, FOC1872277, FOC18X2289, and FOC18Y2296.",
      "center_classification_date": "20200416",
      "distribution_pattern": "Distribution was made to AK, AR, CA, FL, IA, ID, IL, KS, MA, MD, MI, MN, MO, MT, NC, ND, NH, NY, OH, OK, OR, PA, TN, TX, VT, WA, WI, and WV.  There was government and military distribution but no foreign distribution.",
      "state": "CA",
      "product_description": "Canon Aquilion Prime, Model TSX-303A",
      "report_date": "20200422",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Canon Medical System, USA, INC.",
      "recall_number": "Z-1723-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84954",
      "more_code_info": "",
      "recall_initiation_date": "20190325",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}