{
  "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": "83519",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide  Foreign:",
      "recall_number": "Z-2440-2019",
      "product_description": "syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed tomography models:  SOMATOM Definition Edge-Model #10590000;  SOMATOM Definition AS Model #8098027;  SOMATOM Definition Flash Model #10430603",
      "product_quantity": "2867 units worldwide (OUS); 1464 units US",
      "reason_for_recall": "SOMATOM Definition Edge, SOMATOM Definition AS, SOMATOM Definition Flash with software syngo.CT  with Software version VA48A_SP5 may result in scanning workflow interruptions and unexpected user notifications. and may result in a delay in diagnosis and/or patient rescans",
      "recall_initiation_date": "20190725",
      "center_classification_date": "20190830",
      "termination_date": "20221229",
      "report_date": "20190911",
      "code_info": "syngo.CT software version VA48A_SP5.5"
    }
  ]
}