{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89898",
      "recalling_firm": "Roche Diabetes Care, Inc.",
      "address_1": "9115 Hague Rd",
      "address_2": "",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution: AK, AZ, CA, CO, DC, FL, GA, IL, IN, MN, NC, NJ, NY, PA, RI, SC, TX, WI",
      "recall_number": "Z-1008-2022",
      "product_description": "RocheDiabetes Care Platform Software version 2.5.2 material number 08888353001. This is a web application software hosted on a server. There is no physical product.",
      "product_quantity": "81 registered accounts",
      "reason_for_recall": "Potential for patient data mismatch when using browser \"back\" button to navigate between patients when using the diabetes management software.",
      "recall_initiation_date": "20220309",
      "center_classification_date": "20220426",
      "termination_date": "20250122",
      "report_date": "20220504",
      "code_info": "Date of manufacture: 2021-11",
      "more_code_info": ""
    }
  ]
}