{
  "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": "Clearwater",
      "address_1": "5115 Ulmerton Rd",
      "reason_for_recall": "The adhesive may be inadequately applied or the assembly may be manipulated after application of the adhesive resulting in an incomplete bond to the angled tip.",
      "address_2": "",
      "product_quantity": "95",
      "code_info": "Lot 0316D, 0416L, and 0516B.",
      "center_classification_date": "20160824",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of: MD, GA, MO and FL and the country of Finland.",
      "state": "FL",
      "product_description": "BVX-330BR Bovie Precise 360 Handpiece 33cm, blade     Product  is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.",
      "report_date": "20160831",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Bovie Medical Corporation",
      "recall_number": "Z-2646-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74790",
      "termination_date": "20161214",
      "more_code_info": "",
      "recall_initiation_date": "20160718",
      "postal_code": "33760-4004",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}