{
  "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-0109-2018",
      "product_description": "Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T, 866, 866T, 874, 874T, 876, 876T, 884, 886, 886T)",
      "product_quantity": "2,163,610 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: 5188321  5190185  5190186  5184968  5185467  5185468  5185469  5185470  5188322  5188323  5188324  5188325  5188326  5188327  5188328  5189476  5189477  5189478  5189521  5189522  5190187  5190188  5190189  5191046  5191047  5191355  5192532  5183060  5183061  5187300  5187301  5187556  5187557  5189051  5193052  5188329  5188330  5189053  5189054  5194937  5185690  5187558  5191357  5187559"
    }
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}