{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tustin",
      "address_1": "PO Box 2068",
      "reason_for_recall": "It was discovered that the generator of the system could possibly terminate the exposure prematurely during an examination",
      "address_2": "2441 Michelle Dr",
      "product_quantity": "254",
      "code_info": "Model : KXO-80XD",
      "center_classification_date": "20170314",
      "distribution_pattern": "USA ( nationwide ) Distribution to the states of : WA, OR, CA, OH, IL, CT, IA, KY, AL, LA, HI, PA, NJ, DE, MN, DC, NY, MI, SC, MD, TN, OK, WI, UT, ID, NV, TX, AL, IN, WV, KS, MO, CO, MT, MS, NC, GA, NH,UT, FL, AZ and ND.",
      "state": "CA",
      "product_description": "Toshiba Kalare DREX-KL80 X-ray generator",
      "report_date": "20170322",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-1397-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76175",
      "termination_date": "20180614",
      "recall_initiation_date": "20160519",
      "postal_code": "92780-7047",
      "voluntary_mandated": "FDA Mandated",
      "status": "Terminated"
    }
  ]
}