{
  "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": "Seminole",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80012",
      "recalling_firm": "VGI Medical, LLC",
      "address_1": "10401 Belcher Rd S",
      "address_2": "N/A",
      "postal_code": "33777-1415",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to MI, FL, and NY.",
      "recall_number": "Z-2100-2018",
      "product_description": "VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit",
      "product_quantity": "6 units",
      "reason_for_recall": "IFU contained an automated cleaning process for the VerteLP Instrument Tray that was not validated",
      "recall_initiation_date": "20180409",
      "center_classification_date": "20180605",
      "termination_date": "20200821",
      "report_date": "20180613",
      "code_info": "Lots of Instrument Sets: LP-INSTSET-001, VLP-INSTSET-002, VLP-INSTSET-003, VLP-INSTSET-004, VLP-INSTSET-005, VLP-INSTSET-006.    Lots of individual instruments contained in sets: 127617, 127901, 127902, 127903, 127904, 127905, 127906, 127907, 127908, 133003, 133004, 133005, 1330-1, 1330-2, 1330-6, 133004, 1285001, 144301, 144302, 163214, 1401001, 157801, 162402 163203, 163204, 163205, 163206, 163207, 163208, 163209, 163212, 163213, and 163214."
    }
  ]
}