{
  "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": "Birmingham",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86926",
      "recalling_firm": "The Binding Site Group, Ltd.",
      "address_1": "8 Calthorpe Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "U.S.: CO, FL, IA, MA, NC, NJ, NY, OH, SD, and UT.    O.U.S.: Not provided",
      "recall_number": "Z-0943-2021",
      "product_description": "Optilite Freelite Mx Kappa Free Kit  REF LK016.M.OPT.A",
      "product_quantity": "213 kits in the U.S.",
      "reason_for_recall": "Due to customer complaints of positive bias impacting quality control.  The high and low level controls are demonstrating a positive bias compared to assigned values.",
      "recall_initiation_date": "20201118",
      "center_classification_date": "20210201",
      "termination_date": "20241223",
      "report_date": "20210210",
      "code_info": "Model Number: LK016.M.OPT.A  UDI: 05051700019866  Lot Number: 454763",
      "more_code_info": ""
    }
  ]
}