{
  "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": "65432",
      "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": "USA Nationwide including the states of:  FL, CO, Wash DC, VA, KS, TX, OH, TN, OK, CA, IL, MO, and MN.",
      "recall_number": "Z-1664-2013",
      "product_description": "BASE, S-LIFT Instrument Case     Product Usage:  System cases are designed to hold and secure all instrumentation to be used with a surgical system. Case and caddy components are used to contain implants intended for intervertebral body fusion and fixation of the spine.",
      "product_quantity": "12",
      "reason_for_recall": "The S-LIFT Instrument Case contained a bracket with peeling nylon coating.",
      "recall_initiation_date": "20130517",
      "center_classification_date": "20130704",
      "termination_date": "20160517",
      "report_date": "20130710",
      "code_info": "Lot/Serial Numbers:  7201.007 and 7201.007-1"
    }
  ]
}