{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81098",
      "recalling_firm": "OriGen Biomedical, Inc.",
      "address_1": "7000 Burleson Rd Bldg D",
      "address_2": "N/A",
      "postal_code": "78744-3202",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide in the states of NY, AR, MO, NC, GA, LA, CO, AL, MA, CA, MI, TX, OH, MD, FL, TN, SC, OR, AZ, UT, RI, SD, PA, NM, CT.    Foreign (OUS): United Arab Emirates, Kingdom of Saudi Arabia, New Zealand, Thailand",
      "recall_number": "Z-0102-2019",
      "product_description": "Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO",
      "product_quantity": "106",
      "reason_for_recall": "The catheter failed the endotoxin testing.",
      "recall_initiation_date": "20180821",
      "center_classification_date": "20181012",
      "termination_date": "20211005",
      "report_date": "20181024",
      "code_info": "UDI: 00816203022059, lot N18687-1"
    }
  ]
}