{
  "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": [
    {
      "country": "United States",
      "city": "Dover",
      "address_1": "87 Venture Dr",
      "reason_for_recall": "Potential that 3Fr size catheter placed in the catheter tray instead of 4Fr for the 4Fr x 20cm Single Lumen CT  Midline Basic Tray.",
      "address_2": "",
      "product_quantity": "75",
      "code_info": "Product Code: VYML4S1001  Lot Number: 17B012D  Exp. Date: 2021-10-31",
      "center_classification_date": "20191127",
      "distribution_pattern": "One Customer Located in TN",
      "state": "NH",
      "product_description": "4Fr x 20cm Single Lumen CT  Midline Basic Tray, Product Code: VYML4S1001",
      "report_date": "20191204",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.",
      "recall_number": "Z-0585-2020",
      "initial_firm_notification": "",
      "product_type": "Devices",
      "event_id": "84010",
      "termination_date": "20201021",
      "more_code_info": "",
      "recall_initiation_date": "20190924",
      "postal_code": "03820-5914",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}