{
  "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": "2026-04-22",
    "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": "65444",
      "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": "E-Mail",
      "distribution_pattern": "Nationwide Distribution including Texas, Ohio, and Missouri.",
      "recall_number": "Z-1927-2013",
      "product_description": "Invue Split Driver, Assembly with Handle, Model SI70006 Rev G.  Used in conjunction with the Invue Anterior Cervical Plate System under 501(k) clearance number K121060.      The Invue Driver is an instrument consisting of a Radel handle, a shaft and hexalobe-like tip with a 4.0mm split, which allows the driver to collapse to fit into a screw and expand to retain the screw.",
      "product_quantity": "12 devices",
      "reason_for_recall": "Device design.",
      "recall_initiation_date": "20130510",
      "center_classification_date": "20130808",
      "termination_date": "20150720",
      "report_date": "20130814",
      "code_info": "Lot/Serial Numbers: 027104, 027105"
    }
  ]
}