{
  "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": "Lansdale",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81866",
      "recalling_firm": "Vygon U.S.A.",
      "address_1": "2750 Morris Rd Ste A200",
      "address_2": "N/A",
      "postal_code": "19446-6083",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1115-2019",
      "product_description": "Vyon DUALSTOP White Cap used for intravascular lines  Product Code: 9888.002- Product Usage: Cap used for intravascular lines.",
      "product_quantity": "107700",
      "reason_for_recall": "DualStop Caps defect causing leaks in affected product",
      "recall_initiation_date": "20181206",
      "center_classification_date": "20190409",
      "termination_date": "20200512",
      "report_date": "20190417",
      "code_info": "Lot codes:  090718FD  250118FD  081117FD  130218FD  050418FD  020518FD"
    }
  ]
}