{
  "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": "Clearwater",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79398",
      "recalling_firm": "Bovie Medical Corporation",
      "address_1": "5115 Ulmerton Rd",
      "address_2": "N/A",
      "postal_code": "33760-4004",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "worldwide",
      "recall_number": "Z-1155-2018",
      "product_description": "J-Plasma(R) Handpiece, Catalog Numbers: GS-018C, GS-270C, BVX-270B",
      "product_quantity": "5416 units",
      "reason_for_recall": "Bovie Medical is issuing a correction to address incomplete insertion of the J-Plasma(R) handpiece cable plug into the generator receptacle resulting in an incomplete helium seal. The potential exists for patient fluid backflow into the handpiece and the generator receptacle leading to risk of cross-contamination if the generator is reused.",
      "recall_initiation_date": "20180208",
      "center_classification_date": "20180321",
      "termination_date": "20200917",
      "report_date": "20180328",
      "code_info": "All lots manufactured since 01/01/2014"
    }
  ]
}