{
  "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": "2026-04-22",
    "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": "76049",
      "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. distribution to the following; CA, TX, HI, GA, PA, UT, NY, OK, ID, MA, AZ.    Foreign distribution to the following; Australia, Bulgaria, Denmark, Hong Kong, Ireland, Israel, Japan, New Zealand, Taiwan, Belgium, France, Italy, Spain.",
      "recall_number": "Z-1050-2017",
      "product_description": "Human Lambda Free SPAPlus Kit    Product Code: LK018.S    Freelite aids in the detection and monitoring of Multiple Myeloma and related diseases.",
      "product_quantity": "1,002",
      "reason_for_recall": "Calibration curve activity has increased over time in the kit lots listed.",
      "recall_initiation_date": "20121128",
      "center_classification_date": "20170119",
      "termination_date": "20170303",
      "report_date": "20170125",
      "code_info": "Lot #323278, 327963",
      "more_code_info": ""
    }
  ]
}