{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Dover",
      "address_1": "87 Venture Drive",
      "reason_for_recall": "Potential for leaking caused by insufficient bond between needleless device and female luer.",
      "address_2": "",
      "product_quantity": "450",
      "code_info": "1303181  1303100  1304183",
      "center_classification_date": "20150421",
      "distribution_pattern": "Nationwide Distribution including TX, OH, NY, CA, UT, PA, MA, NY, VA, and IL.",
      "state": "NH",
      "product_description": "4\" Microbore T-Port Set, Product Code: BN-448  Accessory device used to administer medical fluids",
      "report_date": "20150429",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Churchill Medical Systems, Inc.",
      "recall_number": "Z-1471-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70369",
      "termination_date": "20160225",
      "more_code_info": "",
      "recall_initiation_date": "20150115",
      "postal_code": "03820-5914",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}