{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Beverly",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66873",
      "recalling_firm": "SpineFrontier, Inc.",
      "address_1": "500 Cummings Ctr Ste 3500",
      "address_2": "N/A",
      "postal_code": "01915-6516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of:Texas, New York, Illinois, Ohio, Virginia, Washington D.C., and  Florida.  .",
      "recall_number": "Z-0555-2014",
      "product_description": "PedFuse Reset Screw Inserters; PedFuse Screw Inserter 08-9 REset Part# 11-80113    The PedFuse Screw Inserter 05-7 REset, Screw Inserter 05-7 REspond, and Screw Inserter 08-9 REset are used as a screw capture, screw driver, and screw insertion tool in the PedFuse system.",
      "product_quantity": "13",
      "reason_for_recall": "Screw inserters may not mate properly with hex interface of the screws.",
      "recall_initiation_date": "20131120",
      "center_classification_date": "20131220",
      "termination_date": "20180626",
      "report_date": "20140101",
      "code_info": "VM13222- 34489",
      "more_code_info": ""
    }
  ]
}