{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tustin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71763",
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "address_1": "PO Box 2068",
      "address_2": "2441 Michelle Dr",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the state of Nevada.",
      "recall_number": "Z-0005-2016",
      "product_description": "Celesteion PCA-9000A/2 PET/CT System",
      "product_quantity": "1",
      "reason_for_recall": "It was found that if specific operations are performed in multi-phase helical scanning, the acquired raw data may not be saved due to a software problem.",
      "recall_initiation_date": "20150508",
      "center_classification_date": "20151007",
      "termination_date": "20151203",
      "report_date": "20151014",
      "code_info": "Model: TSX-301 CI6A with system software V7.0 SPOO04J"
    }
  ]
}