{
  "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": "Terminated",
      "city": "Williamston",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79329",
      "recalling_firm": "Centurion Medical Products Corporation",
      "address_1": "100 Centurion Way",
      "address_2": "N/A",
      "postal_code": "48895-9086",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationally",
      "recall_number": "Z-1086-2018",
      "product_description": "TUBING CHANGE KIT",
      "product_quantity": "N/A",
      "reason_for_recall": "Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.",
      "recall_initiation_date": "20171023",
      "center_classification_date": "20180317",
      "termination_date": "20180621",
      "report_date": "20180328",
      "code_info": "DT6870    Lot codes:  2015110290  2016090890  2017042690"
    }
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}