{
  "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": [
    {
      "status": "Terminated",
      "city": "Glens Falls",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70322",
      "recalling_firm": "Navilyst Medical, Inc",
      "address_1": "10 Glens Falls Technical Park",
      "address_2": "N/A",
      "postal_code": "12801",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.",
      "recall_number": "Z-1184-2015",
      "product_description": "NAMIC Convenience Kit, UPN H749601904231, REF/Catalog No. 60190423, STERILE, Rx ONLY --- For single use only. --- Device Listing Number D136588.    NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.",
      "product_quantity": "1 unit",
      "reason_for_recall": "The labelled expiration dating of the affected product is not fully supported by shelf life verification testing, which may result in a sterility breach. Use of a Fluid Management Convenience Kit, where sterility has been breached, may result in an increased risk of infection.",
      "recall_initiation_date": "20150109",
      "center_classification_date": "20150225",
      "termination_date": "20170310",
      "report_date": "20150304",
      "code_info": "Lot 4802267",
      "more_code_info": ""
    }
  ]
}