{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Tustin",
      "address_1": "PO Box 2068",
      "reason_for_recall": "Toshiba American Medical Systems, Inc. is recalling the TSX-035A because of a potential problem with the Aquilion Lightning CT System iStation cover falling off of the gantry.",
      "address_2": "2441 Michelle Dr",
      "product_quantity": "1 unit",
      "code_info": "Serial No. 2DA15Y2036",
      "center_classification_date": "20160422",
      "distribution_pattern": "US in the state Nevada",
      "state": "CA",
      "product_description": "Aquilion Lightning CT System iStation cover, SID: 70000246, Item Code: TSX-0354A/2D.03    Product Usage:  Aquilion Lightning is a multislice helical CT system that supports whole-body imaging. The system employs Toshiba\u0019s innovative dose-reduction technologies and a fast reconstruction unit designed to minimize the patient exposure dose and improve the workflow. The wide range of advanced applications is designed for operators of all levels of experience, maximizing performance. This device is indicated to acquire and display cross-sectional volumes of the whole body, to include the head. The Aquilion Lightning has the capability to provide volume sets. These volume sets can be used to perform specialized studies, using indicated software/hardware, by a trained and qualified physician.",
      "report_date": "20160504",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-1560-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73857",
      "termination_date": "20160519",
      "recall_initiation_date": "20160412",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}