{
  "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": "64987",
      "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": "US distribution in states of: CO, DC, MA and TX.",
      "recall_number": "Z-1869-2013",
      "product_description": "Caddy - PedFuse, Screw Caddy, 8MM and 9MM, Part Number:  11-80009 Rev. B    The caddy holds, in an organized fashion within the case, 8mm and 9mm pedicle screws used during implantation of pedicle screw system devices intended to provide immobilization and stabilization of spinal segments of skeletally mature patients",
      "product_quantity": "11 caddies",
      "reason_for_recall": "Two sections that are designated for the 8mm and 9mm screws were switched; the holes that hold the 8mm screws are designed for 9mm screws, and the holes that hold the 9mm screws are designated for 8mm screws.",
      "recall_initiation_date": "20121005",
      "center_classification_date": "20130801",
      "termination_date": "20150729",
      "report_date": "20130807",
      "code_info": "31176, 018652, 018645R, 42011",
      "more_code_info": ""
    }
  ]
}