{
  "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": "Louisville",
      "state": "KY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80080",
      "recalling_firm": "Olsen Medical",
      "address_1": "3230 Commerce Center Pl",
      "address_2": "N/A",
      "postal_code": "40211-1900",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution",
      "recall_number": "Z-1943-2018",
      "product_description": "Symmetry Olsen monopolar cord:   (a) Monopolar Cord, 1/8\" Diameter Pin, TUR Connector, 10' (3.0m), REF 92002, QTY 50   (b) Monopolar Cord, Bovie to 90o Female Pin, 10' (3.0m), REF 40-2106, QTY 10  (c) Monopolar Cord, Bovie to 90o Female Pin, 10' (3.0m), REF 40-2110, QTY 10    Designed to bring high frequency electrical power from the electrosurgical generator to the active.",
      "product_quantity": "71,890 devices",
      "reason_for_recall": "Products may encroach into the sterile pouch seal thereby increasing the risk of the seal being compromised.",
      "recall_initiation_date": "20180511",
      "center_classification_date": "20180525",
      "termination_date": "20190415",
      "report_date": "20180606",
      "code_info": "all codes"
    }
  ]
}