{
  "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": [
    {
      "country": "United States",
      "city": "Lansdale",
      "address_1": "2750 Morris Rd Ste A200",
      "reason_for_recall": "Vygon has uncovered potential problems with membrane elasticity in the 896.038, Bionector Needleless connector and is issuing a voluntary recall of the 896.038, Bionector Needleless connector.",
      "address_2": "",
      "product_quantity": "42250",
      "code_info": "Product code and lot numbers: Product Code: 896.038, with lot Numbers: 291113EE, 070214EE, 210314EE, 280314EE.",
      "center_classification_date": "20141022",
      "distribution_pattern": "Worldwide Distribution - US including CA and Internationally to CA.",
      "state": "PA",
      "product_description": "Bionector Needleless connector. Bionector is a multi-purpose catheter accessory; a closed needle-less system permitting blood sampling, intermit ant injection and continuous infusion of fluids or medications to patients in a hospital or homecare situation.",
      "report_date": "20141029",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Vygon Corporation",
      "recall_number": "Z-0113-2015",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "69204",
      "termination_date": "20150330",
      "more_code_info": "",
      "recall_initiation_date": "20140828",
      "postal_code": "19446-6083",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}