{
  "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": "Atlanta",
      "address_1": "400 Perimeter Center Ter Ne",
      "reason_for_recall": "Clinical mistreatment may occur when there are errors in the clinical workflow, or settings are incorrect.",
      "address_2": "Ste 50",
      "product_quantity": "31",
      "code_info": "EM-042, EM7-004, EM-046, EM-060, EM-047, EM-029, EM7-003, EM7-002, EM7-008, EM-062, EM-063, EM3-004, 116001, 116012, 116044, 116055, 116014, 116052, 116023, 116056, 116053, 116043, 116047, 116051, 116122, 116068, 116013, 116046",
      "center_classification_date": "20130904",
      "distribution_pattern": "Nationwide distribution: AL, CT, FL, GA, IA, MS, MO, NJ, NY, ND, OH, OK, PA, RI, TX, VA and Puerto Rico.",
      "state": "GA",
      "product_description": "DMLC IV-ERGO - Beam shaping block for Radiation Therapy.",
      "report_date": "20130911",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-2157-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66048",
      "termination_date": "20150728",
      "more_code_info": "",
      "recall_initiation_date": "20130815",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}