{
  "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": "Walsall",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88545",
      "recalling_firm": "Xstrahl  Limited",
      "address_1": "Unit 2",
      "address_2": "Maybrook Industrial Estate Maybro; Maybrook Road",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US and ALGERIA, AUSTRALIA, AUSTRIA, BULGARIA, CANADA, COSTA RICA, CROATIA, CYPRUS, DENMARK, FRANCE, GERMANY, HONG KONG, IRELAND, ITALY, KAZAKHSTAN, LATVIA, MALTA, MEXICO, NEW ZEALAND, NORWAY, PANAMA, ROMANIA, RUSSIA, SAUDI ARABIA, SPAIN, SWEDEN, SWITZERLAND, UK, UKRAINE",
      "recall_number": "Z-0389-2022",
      "product_description": "Treatment applicator for Gulmay Medical 150 or Xstrahl 150 superficial X-ray therapy system",
      "product_quantity": "120 applicators",
      "reason_for_recall": "Base plate may detach from the main body of the treatment applicator.",
      "recall_initiation_date": "20210827",
      "center_classification_date": "20211216",
      "termination_date": "20260304",
      "report_date": "20211222",
      "code_info": "GM0072, GM0077, GM0086, GM0117, GM0131, GM0158, GM0184, GM0189, GM0275, GM0307, GM0338, GM0379, GM0414, GM0469, GM0506",
      "more_code_info": ""
    }
  ]
}