{
  "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": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "51 Valley Stream Pkwy",
      "reason_for_recall": "There may be an existing dark current phenomenon on ARTISTE LINAC in combination with IMRT or mARC treatments using unflat beams. Software issue.",
      "address_2": "",
      "product_quantity": "3",
      "code_info": "Model number: 08139789, serial numbers: 5419,                                         5784,                                         5830",
      "center_classification_date": "20150318",
      "distribution_pattern": "US Distribution to the states of UT, WI, and NY.",
      "state": "PA",
      "product_description": "ARTISTE MV System, Linear Accelerator (LINAC) with  SysVC10A software.    The intended use of the ARTISTE MV System linear accelerator system is to deliver x-ray radiation for therapeutic treatment of cancer.",
      "report_date": "20150325",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-0984-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69880",
      "termination_date": "20150428",
      "more_code_info": "",
      "recall_initiation_date": "20141119",
      "postal_code": "19355-1406",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}