{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mentor",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71987",
      "recalling_firm": "US Endoscopy Group Inc",
      "address_1": "5976 Heisley Rd",
      "address_2": "N/A",
      "postal_code": "44060-1873",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of: AL, AR, CA, IL, IN, MS, OH, OK & TN.",
      "recall_number": "Z-0001-2016",
      "product_description": "Histolock  Resection Device, US Endoscopy.    An electrosurgical device designed to be used to endoscopically grasp, dissect and transect tissue during gastrointestinal endoscopic procedures.",
      "product_quantity": "41 units",
      "reason_for_recall": "The company has determined the sterility cannot be assured for the affected lot.",
      "recall_initiation_date": "20150714",
      "center_classification_date": "20151001",
      "termination_date": "20161027",
      "report_date": "20151007",
      "code_info": "M/N: 00711117; Lot #: 1505956"
    }
  ]
}