{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Terminated",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80692",
      "recalling_firm": "Encore Medical, Lp",
      "address_1": "9800 Metric Blvd",
      "address_2": "N/A",
      "postal_code": "78758-5445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "U.S. Distribution to states of: AZ, MO, MS, NY, OK, and  UT; internationally to: Japan.",
      "recall_number": "Z-2967-2018",
      "product_description": "Foundation Modular Femoral Stem, Part Number, 220-10-110.  Knee prosthesis component.     The Foundation Revision Knee is a total knee system indicated as knee joint replacement for patients suffering from pain and dysfunction.",
      "product_quantity": "12",
      "reason_for_recall": "After receipt of a product complaint for the labeling, it was determined that this device does not have FDA clearance.",
      "recall_initiation_date": "20180514",
      "center_classification_date": "20180831",
      "termination_date": "20200817",
      "report_date": "20180912",
      "code_info": "All.  Lots-866A1011, 866A1022"
    }
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}