{
  "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": "Glens Falls",
      "address_1": "10 Glens Falls Tech Park",
      "reason_for_recall": "NAMIC Fluid Management Convenience Kits contains a Fluid Delivery Set that was not assembled in accordance with specification, and prevents the device from being used, resulting in a minor delay in procedure.",
      "address_2": "",
      "product_quantity": "38 units",
      "code_info": "Lot Numbers:  5284422  5286610  5283649  5290525  5286542",
      "center_classification_date": "20180417",
      "distribution_pattern": "Recall conducted to end user level.  Recall Notifications were delivered by Fed Express.",
      "state": "NY",
      "product_description": "Fluid Management Convenience Kits (Angioplasty Kits) intended to be used in Fluid Management  and/or Invasive Pressure Monitoring systems.",
      "report_date": "20180425",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Angiodynamics Inc. (Navilyst Medical Inc.)",
      "recall_number": "Z-1390-2018",
      "initial_firm_notification": "",
      "product_type": "Devices",
      "event_id": "79558",
      "termination_date": "20180921",
      "more_code_info": "",
      "recall_initiation_date": "20180118",
      "postal_code": "12801-3864",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}