{
  "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": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76869",
      "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": "Letter",
      "distribution_pattern": "Distributed to: VA, CA, WI",
      "recall_number": "Z-1824-2017",
      "product_description": "Artis zee, Angiographic x-ray system",
      "product_quantity": "3 units distributed in U.S.",
      "reason_for_recall": "Software error - As a result of a software fault in Artis zee systems with software version VD11 and an A100 generator, the possibility exists that following the failure of a tube assembly focus, the Artis system functions properly until the next reactivation.  Following reactivation, the system no longer initializes as intended.",
      "recall_initiation_date": "20170328",
      "center_classification_date": "20170414",
      "termination_date": "20170807",
      "report_date": "20170426",
      "code_info": "Device Model Numbers: 10280959, 10094137, 10094141, Serial numbers: 160449  147208, 153744"
    }
  ]
}