{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Birmingham",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76050",
      "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": "Worldwide Distribution - U.S. (nationwide) and Internationally to the following; Canada, Australia.",
      "recall_number": "Z-1053-2017",
      "product_description": "Freelite Human Lambda Free Kit for use on SPAPLUS    Product Code: LK018.S, LK018.10S  Freelite aids the detection and monitoring of Multiple Myeloma and related diseases",
      "product_quantity": "3,088",
      "reason_for_recall": "A change in the calibration curve causing an increase in false prozone flags.",
      "recall_initiation_date": "20161028",
      "center_classification_date": "20170119",
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      "code_info": "Lot #400012, 400257",
      "more_code_info": ""
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}