{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67558",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "51 Valley Stream Pkwy",
      "address_2": "N/A",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "MN, WI, PA, MI, AL, OH, NC, AR, and NJ.",
      "recall_number": "Z-1309-2014",
      "product_description": "Artis Zee Angiographic x-ray systems.",
      "product_quantity": "9",
      "reason_for_recall": "An inappropriate cable connection was assembled for certain Artis zee systems. which may cause a system failure and possibly lead to a restricted maneuverability of the gantry system.",
      "recall_initiation_date": "20140207",
      "center_classification_date": "20140331",
      "termination_date": "20150316",
      "report_date": "20140409",
      "code_info": "Model numbers: 10094135, 10094137, 10094139, 10094141, 10280959."
    }
  ]
}