{
  "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": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69066",
      "recalling_firm": "Catheter Connections, Inc.",
      "address_1": "615 Arapeen Dr Ste 302A",
      "address_2": "N/A",
      "postal_code": "84108",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of: CT, GA, MD, and PA.    .",
      "recall_number": "Z-2595-2014",
      "product_description": "DualCap IV Pole Strips Disinfectant Caps for Luer Access Valves, REF 500-LB, Sterile.    When left in place for five (5) minutes DualCap Solo\" disinfects needleless luer access valves; thereafter the caps provide a physical barrier to contamination up to ninety-six (96) hours under normal conditions if not removed.",
      "product_quantity": "24,910 units",
      "reason_for_recall": "Catheter Connections is recalling DualCap IV Pole Strips disinfectant caps for luer access valves due to potential improper packaging cap seal which may render the sealed cap non-sterile.",
      "recall_initiation_date": "20140805",
      "center_classification_date": "20140905",
      "termination_date": "20141008",
      "report_date": "20140917",
      "code_info": "Lot 1406509"
    }
  ]
}