{
  "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": "Ongoing",
      "city": "Walsall",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90231",
      "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 Distribution FL, CA, KY",
      "recall_number": "Z-1404-2022",
      "product_description": "X80 RADiant Photoelectric Therapy System",
      "product_quantity": "7 devices; 70 treatment applicators",
      "reason_for_recall": "There is a potential compatibility issue with the systems and replacement treatment applicators.",
      "recall_initiation_date": "20220427",
      "center_classification_date": "20220719",
      "report_date": "20220727",
      "code_info": "Model Number: X80 RADiant Photoelectric Therapy System; Lot Codes: GM0549, GM0567 GM0568, GM0569, GM0570, GM0571 and GM0577; UDI/DI: 5060494200008"
    }
  ]
}