{
  "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": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64407",
      "recalling_firm": "Aesculap, Inc.",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA Nationwide Distribution including the states of:  AR, CA, FL, IN, IA, KS, MD, MN, MO, OR, TN, TX, VA and WA.",
      "recall_number": "Z-0887-2013",
      "product_description": "Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.",
      "product_quantity": "59",
      "reason_for_recall": "The bipolar energy did not stop after release of the foot pedal.",
      "recall_initiation_date": "20130118",
      "center_classification_date": "20130226",
      "termination_date": "20140108",
      "report_date": "20130306",
      "code_info": "Manufacture date on the label on the bottom of the foot pedal - any product with manufactured dates between 45/10 and 31/12"
    }
  ]
}