{
  "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": "If the Apex collimator is incorrectly installed on the radiation head, a touchguard inhibit activates  the view restrictions dialog box only shows the top 12 restrictions.",
      "address_2": "Ste 50",
      "product_quantity": "1",
      "code_info": "152652",
      "center_classification_date": "20130226",
      "distribution_pattern": "Nationwide Distribution including TX",
      "state": "GA",
      "product_description": "Elekta, Apex add-on Micro MLC, collimator for radiation therapy.",
      "report_date": "20130306",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-0885-2013",
      "initial_firm_notification": "Other",
      "product_type": "Devices",
      "event_id": "64213",
      "termination_date": "20140508",
      "recall_initiation_date": "20130118",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}