{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northridge",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78125",
      "recalling_firm": "Medtronic Inc.",
      "address_1": "18000 Devonshire St",
      "address_2": "N/A",
      "postal_code": "91325-1219",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Worldwide",
      "recall_number": "Z-0111-2018",
      "product_description": "Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)",
      "product_quantity": "5,842 units",
      "reason_for_recall": "Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.",
      "recall_initiation_date": "20170910",
      "center_classification_date": "20171118",
      "report_date": "20171129",
      "code_info": "Lot Numbers:  6211649, 6207537"
    }
  ]
}