{
  "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": "Marquette",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73659",
      "recalling_firm": "RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)",
      "address_1": "375 River Park Cir",
      "address_2": "N/A",
      "postal_code": "49855-1781",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic: AL, CO, CT, FL, IN, ID, IL,  MI, MS, MO, NC, NY, TX    Foreign: None  VA/DOD: None",
      "recall_number": "Z-1393-2016",
      "product_description": "RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver",
      "product_quantity": "N/A",
      "reason_for_recall": "Multiple lots of the 26-FNLDRIVER, may have reduced mechanical strength, resulting in driver tip fracturing during use.",
      "recall_initiation_date": "20160318",
      "center_classification_date": "20160414",
      "termination_date": "20160912",
      "report_date": "20160420",
      "code_info": "26-FNLDRIVER, Lot Numbers: 177091, 177093, 183817, 207727, 223926, 227291, 229134, 230523, 232262, 233074, 234205",
      "more_code_info": ""
    }
  ]
}