{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Franklin Lakes",
      "address_1": "1 Becton Dr",
      "reason_for_recall": "Patients are reporting high blood glucose (HBG) levels while using the MiniMed Pro-set and also noticed the catheter of the infusion set was bent/kinked.",
      "address_2": "",
      "product_quantity": "57,750 units",
      "code_info": "6203871 30-Jun-19  6203860 30-Jun-19  6207535 30-Jun-19  6211649 31-Jul-19  6207537 30-Jun-19  6211650 31-Jul-19",
      "center_classification_date": "20170501",
      "distribution_pattern": "US Distribution to the state of : CA",
      "state": "NJ",
      "product_description": "BD FlowSmart Set MiniMed Pro-set Rx Only   Distributed by Medtronic MiniMed  Inc.  8006464633  8185765555    Legal Manufacturer    Becton, Dickinson and Company   USA     BD Medical-Diabetes Care  Becton Dickinson France SAS",
      "report_date": "20170510",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Company",
      "recall_number": "Z-1897-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76294",
      "termination_date": "20171109",
      "more_code_info": "",
      "recall_initiation_date": "20161223",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}