{
  "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": "74031",
      "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": "US nationwide distribution in CA, FL, IN, MI, MO, NC, NY, and TX.",
      "recall_number": "Z-1829-2016",
      "product_description": "Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve.  Spinal fixation device instrument.",
      "product_quantity": "17 devices",
      "reason_for_recall": "Potential for a product defect where the cannula may be obstructed.  This obstruction could prevent a driver from going through, which increases the potential for the driver to slip, resulting in possible patient injury.",
      "recall_initiation_date": "20160422",
      "center_classification_date": "20160526",
      "termination_date": "20170208",
      "report_date": "20160601",
      "code_info": "Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve; Lot Number: 170684; Part Number: 26-COUNTER-T-XLINK"
    }
  ]
}