{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83883",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "N/A",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US in the states of: GA, IN, MO, MS, NJ, OH, PA",
      "recall_number": "Z-0265-2020",
      "product_description": "SOMATOM go.Top, Models 11061640 & 11061648-  a Computer tomography x-ray system",
      "product_quantity": "14 US",
      "reason_for_recall": "SOMATOM go.Top (Models #11061640 & 11061648) with software syngo CT VA20A_SP2 and  active  Guide&GO  license   No dose documentation and no Dose Alert for the special mode  i-  Sequence  during interventional procedures",
      "recall_initiation_date": "20190924",
      "center_classification_date": "20191121",
      "termination_date": "20240708",
      "report_date": "20191127",
      "code_info": "software syngo CT VA20A_SP2 and active  Guide&GO  license"
    }
  ]
}