{
  "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": "Columbia",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69515",
      "recalling_firm": "Vision Rt Inc",
      "address_1": "8840 Stanford Blvd",
      "address_2": "N/A",
      "postal_code": "21045-5827",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution: US distribution in states of: CA, MN, TX, and UT; and internationally to: Republic of Ireland.",
      "recall_number": "Z-0464-2015",
      "product_description": "AlignRT-  Intended for prescription use. The system is indicated for use during simulation, setup and stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body where radiation is indicated.",
      "product_quantity": "7 (Six Units distribited in the US and One in OUS.)",
      "reason_for_recall": "Potential failure of AlignRT to assert interlock.",
      "recall_initiation_date": "20141015",
      "center_classification_date": "20141125",
      "termination_date": "20160510",
      "report_date": "20141203",
      "code_info": "Affected software version:    Software versions 5.0.1738 and 5.0.1742 only.    Affected serial numbers:    248-052, 248-066, 248-088, 249-0059, 249-0133, 249-0134, 249-0139.",
      "more_code_info": ""
    }
  ]
}