{
  "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": [
    {
      "country": "United States",
      "city": "Lake Forest",
      "address_1": "275 N Field Dr",
      "reason_for_recall": "Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore Extension Set, 59 inch with Spin Lock Collar, Non-DEHP, identified above due to a confirmed customer report of an occlusion of solvent in the male luer lock. This occlusion has the potential to prevent the set from being primed for use and cause a delay in therapy.",
      "address_2": "",
      "product_quantity": "48,050 units",
      "code_info": "Product List Number: 14699-28;   Lot Number: 17-077-NS",
      "center_classification_date": "20170111",
      "distribution_pattern": "Nationwide Distribution",
      "state": "IL",
      "product_description": "Minibore Extension Set, 59 Inch with Spin Lock Collar, Non-DEHP, Latex-Free  Intended use: For the administration of drugs and solutions to a patient's vascular system through a vascular access device.",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hospira Inc.",
      "recall_number": "Z-1016-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64220",
      "termination_date": "20170424",
      "more_code_info": "",
      "recall_initiation_date": "20130219",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}