{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Elgin",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85204",
      "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": "E-Mail",
      "distribution_pattern": "US Nationwide distribution. No governmental.",
      "recall_number": "Z-1883-2020",
      "product_description": "Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Product Usage: Probes are used for the fragmentation of urinary/renal and biliary calculi.",
      "product_quantity": "298 boxes. 3 units per box",
      "reason_for_recall": "As part of an investigation into a biocompatibility test discrepancy where a lot failed biocompatibility testing.",
      "recall_initiation_date": "20200310",
      "center_classification_date": "20200504",
      "termination_date": "20210202",
      "report_date": "20200513",
      "code_info": "NTI Catalog Number 9-900-54.",
      "more_code_info": ""
    }
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}