{
  "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": "67956",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "51 Valley Stream Pkwy",
      "address_2": "",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of AL, ME, PA, IL, and CA.",
      "recall_number": "Z-1652-2014",
      "product_description": "Siemens Linear Accelerator (LINAC) models.     Product Usage:  deliver X-ray radiation for therapeutic treatment of cancer",
      "product_quantity": "9",
      "reason_for_recall": "Siemens Radiation Oncology became aware that customers may be using the Siemens Linear Accelerator in combination with stereotactic accessories which have not been validated as being compatible with Siemens LINAC models.",
      "recall_initiation_date": "20140401",
      "center_classification_date": "20140523",
      "termination_date": "20150316",
      "report_date": "20140604",
      "code_info": "material numbers and serial numbers: 1940035 2962  8139789 5833  8139789 5899  9401654 2113  1940035 2628  4504200 3066  4504200 3361  1940035 3873  1940035 2855",
      "more_code_info": ""
    }
  ]
}