{
  "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": "66314",
      "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": "Worldwide Distribution -  USA (nationwide) and Internationally to Canada.",
      "recall_number": "Z-0140-2014",
      "product_description": "Siemens RAD Fluoro Uro system (Luminos dRF and Uroskop Omnia with software version VD10A/G    Image intensified Fluoroscopic X-ray system",
      "product_quantity": "59",
      "reason_for_recall": "When using systems operating with software versions VD10A/G during a RAD examination, a malfunction can result in radiation continuing longer than required resulting in an overexposed image that is not of diagnostic quality, prompting repetition of the examination.",
      "recall_initiation_date": "20130903",
      "center_classification_date": "20131127",
      "termination_date": "20150309",
      "report_date": "20131204",
      "code_info": "Model numbers 10094910 and 10094200 with software version VD10A/G."
    }
  ]
}