{
  "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": "65429",
      "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": "Letter",
      "distribution_pattern": "USA Nationwide Distribution including the states of:  FL, TX, OK, MO, NJ, MA",
      "recall_number": "Z-1665-2013",
      "product_description": "S-LIFT Inserter Outer Sleeve     Product Usage:  The Inserter Sleeve is an optional instrument to add further compression of the Inserter into the Implant during implantation of S-LIF Intervertebral Body Fusion Devices using bone graft to facilitate fusion of the spine of skeletally mature patients. Model: SI50003 RevA",
      "product_quantity": "12 devices",
      "reason_for_recall": "The outer sleeve would not fit over the S-LIFT Inserter assembly because the hole at the top of the sleeve handle was too small.",
      "recall_initiation_date": "20130524",
      "center_classification_date": "20130704",
      "termination_date": "20141008",
      "report_date": "20130710",
      "code_info": "Lot/Serial Numbers: 47175"
    }
  ]
}