{
  "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": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72216",
      "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": "Letter",
      "distribution_pattern": "US Distribution to the states of : SC, WI, RI, NY, MO, AR, OK, GA, FL, AL, CA, AZ and CO.",
      "recall_number": "Z-0165-2016",
      "product_description": "Exprt Precision System: Revision Knee, Model Number 160-010-726/738    For use with the Exprt Knee System in total knee arthroplasty to replace the native patella.",
      "product_quantity": "209 units",
      "reason_for_recall": "The labeling is missing the size/diameter information.",
      "recall_initiation_date": "20150916",
      "center_classification_date": "20151026",
      "termination_date": "20160104",
      "report_date": "20151104",
      "code_info": "471T1-001/011; 472T1-000/014; 473T1-000/015; 474T1-000/010; 475T1-000/008"
    }
  ]
}