{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tustin",
      "address_1": "2441 Michelle Dr",
      "reason_for_recall": "Toshiba America Medical Systems, Inc. initiated this recall due to the failure of the parts used in the X-ray high-voltage generator. In some cases, X-ray exposure cannot be performed.",
      "address_2": "P.O. Box 2068",
      "product_quantity": "8 units",
      "code_info": "SERIAL NO.:  1CB1262006,  1DB1312033,  1DC1352070,  1DB1342060,  1DB1332049,  1DC1382081,  1DB1312027,  1DB1332045,  1DC1362073,  1CB12X2018.",
      "center_classification_date": "20140306",
      "distribution_pattern": "US Distribution including the states of: MD, WV, OH, CA, MN, IN, NY and WI.",
      "state": "CA",
      "product_description": "TSX-301C Aquilion One (Vision Edition) Computed Tomography X-Ray System.",
      "report_date": "20140312",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-0972-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67227",
      "termination_date": "20141016",
      "more_code_info": "",
      "recall_initiation_date": "20131211",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}