{
  "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": "Northridge",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74955",
      "recalling_firm": "Medtronic Inc.",
      "address_1": "18000 Devonshire Street",
      "address_2": "N/A",
      "postal_code": "91325-1219",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution to TN, MN, and WA",
      "recall_number": "Z-2898-2016",
      "product_description": "CareLink iPro Version 1.10, Catalog No. MMT-7340  With data obtained from the iPro2 recorder and blood glucose meter, the CareLink iPro software retrospectively calibrates sensor data and provides reports of continuous glucose information. CareLink iPro reports show up to seven calendar days of study data. The reports are created in PDF format, so they can easily be printed or stored electronically.",
      "product_quantity": "33 units",
      "reason_for_recall": "Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software due to a time stamp error.",
      "recall_initiation_date": "20160805",
      "center_classification_date": "20160927",
      "termination_date": "20161020",
      "report_date": "20161005",
      "code_info": "n/a"
    }
  ]
}