{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Arlington",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86278",
      "recalling_firm": "Wright Medical Technology Inc",
      "address_1": "11576 Memphis Arlington Rd",
      "address_2": "N/A",
      "postal_code": "38002-9497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA  states: CA, CO, FL, GA, MA, MO, OH, PA, TX    OUS: Australia, Canada, Chile, Israel, Spain",
      "recall_number": "Z-2989-2020",
      "product_description": "EVOLVE STEM 8.5MM  Model # 496S085",
      "product_quantity": "16 stems",
      "reason_for_recall": "Lack of sterility assurance",
      "recall_initiation_date": "20200826",
      "center_classification_date": "20200921",
      "termination_date": "20210427",
      "report_date": "20200930",
      "code_info": "Lot # 1668777"
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}