{
  "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": "80666",
      "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": "The devices were not distributed in the United States.    The devices were distributed to the following foreign countries:  Great Britain.",
      "recall_number": "Z-2949-2018",
      "product_description": "P.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830",
      "product_quantity": "1",
      "reason_for_recall": "This unit may be missing the screw/collet Assembly",
      "recall_initiation_date": "20180718",
      "center_classification_date": "20180829",
      "termination_date": "20190417",
      "report_date": "20180905",
      "code_info": "Lot: C2KJ24, GTIN: 10603295234135"
    }
  ]
}