{
  "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": "Jupiter",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73657",
      "recalling_firm": "Atlas Spine, Inc.",
      "address_1": "1555 Jupiter Park Dr Ste 4",
      "address_2": "N/A",
      "postal_code": "33458-8085",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution to FL, MO, and WV.",
      "recall_number": "Z-1616-2016",
      "product_description": "Atlas Spine Torque Limiting Handle 6N-m, P/N 70089 Model # ITN-001-000  Used to rotate implant into position",
      "product_quantity": "16",
      "reason_for_recall": "The device was not appropriately set to mitigate the risk of implant fracture upon rotation inside the disc space.",
      "recall_initiation_date": "20130726",
      "center_classification_date": "20160506",
      "termination_date": "20190726",
      "report_date": "20160518",
      "code_info": "Lots #:  8887, 000073, 000135, 00434, and 02518."
    }
  ]
}