{
  "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": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "Hardware issue that may expose the User to a potential risk for serious injury due to exposure to rotating or electrical parts.",
      "address_2": "",
      "product_quantity": "57 systems distributed in USA",
      "code_info": "Model Numbers: 8098027  10430603",
      "center_classification_date": "20161108",
      "distribution_pattern": "Nationwide Distribution",
      "state": "PA",
      "product_description": "SOMATOM Definition AS  system, x-ray, tomography, computed",
      "report_date": "20161116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-0373-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75509",
      "termination_date": "20170313",
      "more_code_info": "",
      "recall_initiation_date": "20161019",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}