{
  "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": "Redmond",
      "state": "WA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63253",
      "recalling_firm": "Gynex Corporation",
      "address_1": "14603 NE 87th St.",
      "address_2": "N/A",
      "postal_code": "98052",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-0008-2013",
      "product_description": "Sterile, single-use, disposable electrosurgical electrode holder.  It connects the electrode to the foot activated electric generator.  Label reads in part \"***GYNEX*** Electrode Handpiece, Foot Activated*** Manufactured for GYNEX***\"    Gynex catalog number:  950 (Gynex REF 950, Electrode Handpiece)    It connects the electrode to the food activated electric generator. Electrodes are used in gynecological procedures, in a physician's office, for cutting to remove tissue and coagulation to control bleeding by the use of high frequency current.",
      "product_quantity": "19 boxes (containing 12 electorde hand pieces each)",
      "reason_for_recall": "The wrong electrical connector pin was attached to the cord during assembly by the manufacturer.  this electrical connector is too big to fit into the port on the foot activated generator.  this makes the device unusable.",
      "recall_initiation_date": "20120906",
      "center_classification_date": "20121003",
      "termination_date": "20121022",
      "report_date": "20121010",
      "code_info": "Manufacturer's lot number:  54-12-2-21-12."
    }
  ]
}