{
  "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": "66231",
      "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-0374-2014",
      "product_description": "(Siemens Rad Fluoro Uro Systems) Ysio, Luminos Agile, Luminos dRF, and Uroskop Omnia systems with software version VC10    Image intensified fluoroscopic x-ray system",
      "product_quantity": "357",
      "reason_for_recall": "A potential malfunction and hazard to patients exists when using the Ysio, Luminos Agile, Luminos dRF, and Uroskop Omnia systems with software version VC10, which may result in radiation continuing longer than required and overexposed images that are not of diagnostic quality.",
      "recall_initiation_date": "20130903",
      "center_classification_date": "20131126",
      "termination_date": "20150224",
      "report_date": "20131204",
      "code_info": "Model numbers: 10094200, 10094910, 10281013, 10281163, 10502200"
    }
  ]
}