{
  "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": "Austin",
      "address_1": "7000 Burleson Rd",
      "reason_for_recall": "Potential for clear extension tube to separate from the hub, which could result in blood loss and may require intervention to prevent permanent impairment/damage.",
      "address_2": "Bldg D",
      "product_quantity": "51 units",
      "code_info": "Lot N18549",
      "center_classification_date": "20150423",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and countries of: Spain, UK, Germany, Sweden, and Netherlands.",
      "state": "TX",
      "product_description": "OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter STERILE DISPOSABLE: DO NOT RE-USE Manufactured by: OriGen Biomedical.       OriGene VV13F Reinforced Dual Lumen Catheter indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures of six hours or less.",
      "report_date": "20150429",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "OriGen Biomedical, Inc.",
      "recall_number": "Z-1456-2015",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "70988",
      "termination_date": "20160503",
      "more_code_info": "",
      "recall_initiation_date": "20150330",
      "postal_code": "78744-3202",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}