{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Martinez",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64675",
      "recalling_firm": "Siemens Medical Solutions USA,  Inc",
      "address_1": "757 Arnold Dr Ste A",
      "address_2": "N/A",
      "postal_code": "94553-3615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution",
      "recall_number": "Z-1044-2013",
      "product_description": "SIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B; Software release for COHERENCE Therapist 2.3 for Primus and Oncor Linear Accelerators;     Model:  Primeview 3i  2.0, Part No.\t\t\t \t 8139847,   Current R630;    Product Usage:  The intended use of the SIEMENS branded ONCOR\u001d and PRIMUS\u001d family of linear accelerator systems is to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer.",
      "product_quantity": "621 units (foreign account) in total",
      "reason_for_recall": "Siemen's issued a Customer Information Letter under Update Instruction TH016/12S to alert all its affected customers of the software issues. The software release is a result of the final system testing addressing multiple performance defects and several safety issues that were not considered critical (for immediate correction) for the safe use of the device.",
      "recall_initiation_date": "20130305",
      "center_classification_date": "20130401",
      "termination_date": "20140828",
      "report_date": "20130410",
      "code_info": "All units of these models."
    }
  ]
}