{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72789",
      "recalling_firm": "ArthroCare Corporation",
      "address_1": "7000 W William Cannon Dr",
      "address_2": "N/A",
      "postal_code": "78735-8509",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution.  US nationwide including OH, MO, AZ, AL, CA, FL, SC, GA, and PA; Spain, France, United Kingdom, Germany, Switzerland, Singapore, Russia, Turkey, and Ecuador.",
      "recall_number": "Z-0623-2016",
      "product_description": "Cavity 8 Gauge Spine Wand indicated for resection, ablation, and coagulation of soft tissues and hemostasis of blood vessels in spinal procedures.",
      "product_quantity": "262 units",
      "reason_for_recall": "There is cracking in the tray when the device is snapped into place. The crack is through the full thickness of the tray, compromising the sterile barrier.",
      "recall_initiation_date": "20151026",
      "center_classification_date": "20160108",
      "termination_date": "20160623",
      "report_date": "20160120",
      "code_info": "Lot Numbers: 1024313, 1024482, 1027160, 1034306, 1041879, 1059328"
    }
  ]
}