{
  "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": "66698",
      "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": "N/A",
      "distribution_pattern": "US Distribution to VA and TX.",
      "recall_number": "Z-0544-2014",
      "product_description": "PedFuse Reset Screw; Model: 01-80115-55    The PedFuse Reset pedicle screw implants intended to be used to help provide immobilization and stabilization of spinal segments as an adjunct to fusion of the thoracic, lumbar, and/or sacral spine.",
      "product_quantity": "35 Devices",
      "reason_for_recall": "During routine servicing, it was discovered that one 8mmx55mm Reset screw was assembled with an 8mm tulip head and a 9mm screw. The implant should have  consisted of an 8mm tulip head and an 8mm screw. A recall was initiated to remove all remaining screws of the same lot from the field to investigate the nonconformity.",
      "recall_initiation_date": "20131018",
      "center_classification_date": "20131219",
      "termination_date": "20160822",
      "report_date": "20131225",
      "code_info": "Lot/Serial Numbers: 357305-000"
    }
  ]
}