{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Abingdon",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90654",
      "recalling_firm": "OXFORD IMMUNOTEC LTD",
      "address_1": "143 Park Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: AL, CA, DC, GA, IN, OR, and WA  O.U.S.: None",
      "recall_number": "Z-1642-2022",
      "product_description": "T-Cell Xtend REF TTK.610 US",
      "product_quantity": "47 units",
      "reason_for_recall": "Due to equipment failure, affected products were stored at temperatures outside the validated range of 2-8 degree C for a period longer than the validated storage time.",
      "recall_initiation_date": "20220707",
      "center_classification_date": "20220826",
      "report_date": "20220907",
      "code_info": "Model/Catalog Number: TTK.610 US UDI-DI Code: 15051716000022 Lot Number: 1001",
      "more_code_info": ""
    }
  ]
}