{
  "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": "Terminated",
      "city": "Birmingham",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76131",
      "recalling_firm": "The Binding Site Group, Ltd.",
      "address_1": "8 Calthorpe Road",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. distribution to the following; FL, TX, PA, CA, MA, WA, MI, CT.     No foreign distribution.",
      "recall_number": "Z-1089-2017",
      "product_description": "Optilite IgG4 Kit  Product Code: LK009.OPT.A",
      "product_quantity": "9 users",
      "reason_for_recall": "A change to the lower end of the measuring range and product insert did not reflect the change.The measuring range provided in instrument parameters is correct but contradicts the information provided in the product insert",
      "recall_initiation_date": "20161223",
      "center_classification_date": "20170124",
      "termination_date": "20170503",
      "report_date": "20170201",
      "code_info": "Lot #401413"
    }
  ]
}