{
  "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": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79072",
      "recalling_firm": "DePuy Orthopaedics, Inc.",
      "address_1": "325 Paramount Dr",
      "address_2": "N/A",
      "postal_code": "02767-5199",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-0848-2018",
      "product_description": "Concorde Lift Driver Shaft AO.    Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.",
      "product_quantity": "130 units total",
      "reason_for_recall": "Potential for Intra-operative breakage of driver tips",
      "recall_initiation_date": "20170726",
      "center_classification_date": "20180302",
      "termination_date": "20190403",
      "report_date": "20180314",
      "code_info": "Product code: 287804101G  Lot number: 052316-A R, 121416-A R"
    }
  ]
}