{
  "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": [
    {
      "country": "United States",
      "city": "Center Valley",
      "address_1": "3773 Corporate Pkwy",
      "reason_for_recall": "Complaints were received for the GN161 Bipolar Foot Control reporting that the bipolar energy did not stop after release of the foot control.",
      "address_2": "",
      "product_quantity": "85",
      "code_info": "all GN161's distributed between 4/28/2009 and 5/22/2013.",
      "center_classification_date": "20131210",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide and countries of: Austria, Germany, Japan, and Taiwan.",
      "state": "PA",
      "product_description": "Aesculap GNI161 Bipolar Foot Control    Product Usage:  The Aesculap Bipolar Coagulator is intended for use in surgery to generate electrical power for bipolar instruments. Bipolar coagulators are used in neurosurgery, ENT surgery, urology, laparoscopy, and plastic surgery.",
      "report_date": "20131218",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Aesculap, Inc.",
      "recall_number": "Z-0479-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66533",
      "termination_date": "20141020",
      "more_code_info": "",
      "recall_initiation_date": "20130910",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}