{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75608",
      "recalling_firm": "DePuy Orthopaedics, Inc.",
      "address_1": "700 Orthopaedic Dr",
      "address_2": "N/A",
      "postal_code": "46582-3994",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution in the state of TN",
      "recall_number": "Z-0703-2017",
      "product_description": "LCS Complete Knee Revision System VVC Insert    Product Usage:  LCS VVC Insert is used in Knee Revision Surgery",
      "product_quantity": "1",
      "reason_for_recall": "DePuy Orthopaedics, Inc. is voluntarily recalling one lot of the LCS Complete Knee Revision System VVC Insert Small 22.5mm, due to the insert being manufactured outside of  specifications, which prevents the insert from properly seating in the mating tibial tray.",
      "recall_initiation_date": "20161108",
      "center_classification_date": "20161203",
      "termination_date": "20170605",
      "report_date": "20161214",
      "code_info": "LCS COMP VVC INS SM 22.5MM, Product Code: 129424122, Lot# C08294,  GTIN: (01)10603295024484, Expiry: 31-Mar-2021"
    }
  ]
}