{
  "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": "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": "2350",
      "code_info": "1303123  1305003  1305008  1305049  1306097",
      "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 Double Lumen Set with Bionector, Product Code: BN-208  Accessory device used to administer medical fluids",
      "report_date": "20150429",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Churchill Medical Systems, Inc.",
      "recall_number": "Z-1469-2015",
      "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"
    }
  ]
}