{
  "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": "2026-04-29",
    "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": "68633",
      "recalling_firm": "Medtronic MiniMed Inc.",
      "address_1": "18000 Devonshire St",
      "address_2": "N/A",
      "postal_code": "91325-1219",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "New Jersey and Worldwide: Belgium, France, Netherland, and Sweden",
      "recall_number": "Z-2173-2014",
      "product_description": "Medtronic MiniMed Implantable Insulin Pump, Model No. MMT-2007D",
      "product_quantity": "764 units",
      "reason_for_recall": "Medtronic MiniMed is recalling the Implantable Insulin Pump because there have been reports of a pump malfunction resulting in the disconnection of the delivery of insulin prior to the end of the 7 year useful life of the device.",
      "recall_initiation_date": "20140616",
      "center_classification_date": "20140808",
      "termination_date": "20140925",
      "report_date": "20140820",
      "code_info": "n/a"
    }
  ]
}