{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Stockholm",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88771",
      "recalling_firm": "ELEKTA SOLUTIONS AB",
      "address_1": "Box 7593",
      "address_2": "KUNGSTENSGATAN 18",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was to ND and NC.  There was no military/government distribution.",
      "recall_number": "Z-0115-2022",
      "product_description": "Elekta Medical Linear Accelerator (EMLA):    Elekta Harmony Pro, REF 1555143; Elekta Infinity, REF 1552091, and Elekta Versa HD, REF 1552093.",
      "product_quantity": "2 in the U.S.",
      "reason_for_recall": "There is a risk that the Diode D1 in the Modulator can fail in a destructive manner when removed from the machine, and that the protective tube surrounding the diode may fail to contain the ejected matter.",
      "recall_initiation_date": "20210928",
      "center_classification_date": "20211014",
      "termination_date": "20240614",
      "report_date": "20211020",
      "code_info": "Elekta Harmony Pro, Serial #441009, UDI (01) 05060191071604;  Elekta Infinity, Serial #156645, UDI (01) 05060191071543; and  Elekta Versa HD, Serial #156646, #156477, and #156648,  UDI (01) 05060191071574"
    }
  ]
}