{
  "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": [
    {
      "country": "United States",
      "city": "Martinez",
      "address_1": "757 Arnold Dr Ste A",
      "reason_for_recall": "The potential for a safety issue, for the image quality degradation, that is addressed by the Customer Safety Advisory Notice when verifying the patient position based on 2D images that were acquired as single-exposure MV or In-Line kView images using the syngo RT Therapist 4.3.",
      "address_2": "",
      "product_quantity": "8 units",
      "code_info": "All units of the version 4.3, Part No. 08162815",
      "center_classification_date": "20130620",
      "distribution_pattern": "Worldwide distribution",
      "state": "CA",
      "product_description": "ARTISTE with syngo RT Therapist  version 4.3    Product Usage:  The intended use of the SIEMENS branded ARTISTE family of linear accelerator systems is to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer.",
      "report_date": "20130626",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA,  Inc",
      "recall_number": "Z-1562-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65435",
      "termination_date": "20131126",
      "more_code_info": "",
      "recall_initiation_date": "20130529",
      "postal_code": "94553-3615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}