{
  "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": "88921",
      "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": "Letter",
      "distribution_pattern": "U.S.: CA, CO, FL, IL, IN, KY, LA, MI, NY, OK, SD, TX and VA.     O.U.S.: Canada",
      "recall_number": "Z-0274-2022",
      "product_description": "Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S  Freelite Human Lambda Free Kit (for use on the SPAPLUS) (x10) REF LK018.10S",
      "product_quantity": "2,254 kits",
      "reason_for_recall": "Due to calibration curves producing a higher activity than routinely expected and that there may be a decrease in separation between calibrator point 5 and calibrator point 6, which can be exacerbated with calibrator 6 activity reaches the optical ceiling of the SPA+ analyzer.",
      "recall_initiation_date": "20211015",
      "center_classification_date": "20211119",
      "termination_date": "20250204",
      "report_date": "20211201",
      "code_info": "Model Number: LK018.S UDI Code: 05051700006477 Lot Number: 472776  Model Number:LK018.10S UDI Code: 05051700012201 Lot Number: 472664",
      "more_code_info": ""
    }
  ]
}