{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Beverly",
      "address_1": "500 Cummings Ctr Ste 3500",
      "reason_for_recall": "Bone Probes used to create a pathway in pedicle bone were manufactured and marked to incorrect specifications.",
      "address_2": "",
      "product_quantity": "13 devices",
      "code_info": "Lot:  012212-001",
      "center_classification_date": "20140103",
      "distribution_pattern": "US Distribution: including states of: TX and VA.",
      "state": "MA",
      "product_description": "PedFuse Bone Probe; Part: SI81008 spinal pedicle fixation.",
      "report_date": "20140115",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "SpineFrontier, Inc.",
      "recall_number": "Z-0624-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "66273",
      "termination_date": "20141008",
      "more_code_info": "",
      "recall_initiation_date": "20130911",
      "postal_code": "01915-6516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}