{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Elgin",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90095",
      "recalling_firm": "Northgate Technologies, Inc.",
      "address_1": "1591 Scottsdale Ct",
      "address_2": "",
      "postal_code": "60123-9361",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of MA.",
      "recall_number": "Z-1235-2022",
      "product_description": "AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe",
      "product_quantity": "55 probes",
      "reason_for_recall": "Product labeled incorrectly.",
      "recall_initiation_date": "20220413",
      "center_classification_date": "20220603",
      "termination_date": "20221108",
      "report_date": "20220615",
      "code_info": "NTI Catalog Number 72-00322-0 / BSC Catalog No. M00546620; Lot code: BSC15876; GTIN: 00817183020448.",
      "more_code_info": ""
    }
  ]
}