{
  "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": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68552",
      "recalling_firm": "RGI Medical Manufacturing, Inc.",
      "address_1": "4637 NW 6th St",
      "address_2": "",
      "postal_code": "32609-0701",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of AL, CA, DE, GA, IL, KY, MA, MD, ME, MI, MN, NJ, NM, NV, NY, OH, TN, TX, WA, and WI.",
      "recall_number": "Z-1996-2014",
      "product_description": "Henora REF: 70-4026-09V1  300psi I.V. Catheter Extension Set      Product Usage:  Catheter extension set for high pressure procedures.",
      "product_quantity": "19,200 units.",
      "reason_for_recall": "Problem with low adhesion of the tubing to luer connection  which may lead to a separation of the extension set while in use.",
      "recall_initiation_date": "20140328",
      "center_classification_date": "20140706",
      "termination_date": "20160929",
      "report_date": "20140716",
      "code_info": "Lot numbers 102131 and 110531.",
      "more_code_info": ""
    }
  ]
}