{
  "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": [
    {
      "country": "United States",
      "city": "Rancho Santa Margarita",
      "address_1": "22872 Avenida Empresa",
      "reason_for_recall": "Potential to improperly characterize tissue within the jaws, which may result in nonoptimal power delivery.",
      "address_2": "",
      "product_quantity": "101 units (U.S) and 38 units (International)",
      "code_info": "Model Number: EB040   Lot Numbers: 1243964, 1243975, 1244125    Model Number: EB040+  Lot Numbers: 1245512, 1245513, 1246241, 1246508, 1247079, 1247566, 1248102, 1249264",
      "center_classification_date": "20150915",
      "distribution_pattern": "Worldwide Distribution - U.S Nationwide in the states of:FL, GA, NV. and countries of: France, Netherlands, Spain, and United Kingdom.",
      "state": "CA",
      "product_description": "Voyant Open Fusion Device  Models: EB040 and EB040+    Product Usage:  The Applied Voyant Open Fusion Device is designed for use with the Voyant Electrosurgical Generator. The device is an advanced bipolar instrument that uses RF energy, provided by the generator, to seal vessels up to and including 5mm (EB040+) or 7mm (EB040) in diameter. The device may also be used to seal tissue bundles that can be captured in the device jaws. The system delivers the energy required to fuse the tissue between the jaws of the device by monitoring voltage and current throughout the seal cycle. The device also features a useractuated blade for the transection of sealed tissue.",
      "report_date": "20150923",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Applied Medical Resources Corp",
      "recall_number": "Z-2769-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71956",
      "termination_date": "20151120",
      "more_code_info": "",
      "recall_initiation_date": "20150731",
      "postal_code": "92688-2650",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}