{
  "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": "76023",
      "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": "Nationwide Distribution to:  AZ  CA  IA  IL  IN  LA  MA  MD  ME  MI  MN  PA  VA",
      "recall_number": "Z-2317-2017",
      "product_description": "DePuy Synthes   various orthopedic instruments modified by U.S. Distributors  These instruments are used in various orthopedic procedures",
      "product_quantity": "345",
      "reason_for_recall": "Products were made outside of Quality System Regulation, and potentially outside of premarket submission (510k/PMA) for certain devices.  The safety or effectiveness of these devices cannot be assured.",
      "recall_initiation_date": "20170106",
      "center_classification_date": "20170608",
      "termination_date": "20190515",
      "report_date": "20170614",
      "code_info": "Unknown"
    }
  ]
}