{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Crawley",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81886",
      "recalling_firm": "Elekta Limited",
      "address_1": "Linac House",
      "address_2": "Fleming Way",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "TX and WI, Germany, Denmark, Netherlands, United Kingdom",
      "recall_number": "Z-0706-2019",
      "product_description": "Elekta Unity",
      "product_quantity": "2 units",
      "reason_for_recall": "In rare circumstances, due to reasons such as inadequate hospital facility maintenance, water leakage, and weakening of speaker fixings during the lifetime of the system, the speakers can become dislodged and be pulled into the bore.",
      "recall_initiation_date": "20190104",
      "center_classification_date": "20190109",
      "report_date": "20190116",
      "code_info": "Serial Numbers:  1536549, 1536549",
      "more_code_info": ""
    }
  ]
}