{
  "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": "Elgin",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77367",
      "recalling_firm": "Northgate Technologies, Inc.",
      "address_1": "1591 Scottsdale Ct",
      "address_2": "N/A",
      "postal_code": "60123-9361",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the following states :  MA, NE and  TN  and Internationally  to Canada.",
      "recall_number": "Z-0073-2018",
      "product_description": "Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9-201-00 Autolith lithotripter. electrohydraulic lithotripsy (EHL) is a method that allows large stones to be fragmented and removed percutaneously or endoscopically.",
      "product_quantity": "186",
      "reason_for_recall": "The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to Northgate Technologies, the resistor in the probe will not allow the mislabeled product to be used with the incorrect generator. Could Delay Care.",
      "recall_initiation_date": "20170524",
      "center_classification_date": "20171108",
      "termination_date": "20200609",
      "report_date": "20171115",
      "code_info": "Model No. 9-195-371DS, Lot/Serial Number LDS12516"
    }
  ]
}