{
  "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": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84518",
      "recalling_firm": "Roche Diabetes Care, Inc.",
      "address_1": "9115 Hague Rd",
      "address_2": "N/A",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide:  Foreign: Austalia, India",
      "recall_number": "Z-0999-2020",
      "product_description": "ACCU-CHEK AVIVA ASPAC STRIP 50CT- intended for Blood Glucose Monitoring System  Catalog Number:  06453970020",
      "product_quantity": "61,329 units  (OUS)",
      "reason_for_recall": "Inability to dose the test strips, may result in a temporary inability to get a result that could lead to a delay in treatment and/or therapy decisions",
      "recall_initiation_date": "20191211",
      "center_classification_date": "20200205",
      "termination_date": "20220708",
      "report_date": "20200212",
      "code_info": "Lot Number: 498287"
    }
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}