{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "41220",
      "product_res_number": "Z-0162-06",
      "event_date_initiated": "2005-04-27",
      "event_date_posted": "2005-11-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-03-20",
      "res_event_number": "33025",
      "product_code": "LZG",
      "product_description": "''Fine Tuning Your Pump'' booklet provided with Model MMT-515 AND MMT-715 INSULIN INFUSION PUMPS",
      "code_info": "All Models MMT-515 and MMT-715 shipped between 10/01/2004 and 04/05/2005",
      "firm_fei_number": "3003166194",
      "recalling_firm": "Medtronic MiniMed",
      "address_1": "18000 Devonshire St",
      "city": "Northridge",
      "state": "CA",
      "postal_code": "91325-1219",
      "reason_for_recall": "The text description of how to perform insulin sensitivity testing and associated worksheet included in the booklet that is shipped with the Paradigm 515 and Paradigm 715 insulin pumps contained a basic flaw in that the blood glucose after the correction should be compared to the target glucose and it says compare to the beginning blood glucose in the procedure.",
      "root_cause_description": "Other",
      "action": "All end users who recieved the model MMT-515 or MMT-715 pump that included the 'Fine Yuning Your Pump' workbook will be notified through a letter.",
      "product_quantity": "Approximately 14,560",
      "distribution_pattern": "Nationwide,  Bahamas, Bermuda, Canada, Mexico, and Puerto Rico.",
      "openfda": {
        "k_number": [
          "K111669",
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          "K993012",
          "K043000",
          "K063126",
          "K093364",
          "K994186",
          "K013309",
          "K040676",
          "K031738",
          "K080639",
          "K182630",
          "K042873",
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        ],
        "registration_number": [
          "3010291427",
          "3012421607",
          "2029275",
          "3013636348",
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          "3020976354",
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        ],
        "fei_number": [
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          "3013636348",
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          "1313700",
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          "3011393376",
          "1000306431",
          "3002806559",
          "3001058982",
          "3007871880",
          "3002806818",
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          "2246552",
          "3003024060",
          "3004173703",
          "3009337401",
          "3020976354",
          "3015218509",
          "3008824097",
          "3006479639",
          "3010162782",
          "3002558692",
          "3005340341"
        ],
        "device_name": "Pump, Infusion, Insulin",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5725",
        "device_class": "2"
      }
    }
  ]
}