{
  "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": "Lawrence",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72543",
      "recalling_firm": "NxStage Medical, Inc.",
      "address_1": "350 Merrimack Street",
      "address_2": "N/A",
      "postal_code": "01843-1748",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution.  US Nationwide, Netherlands, and Sweden.",
      "recall_number": "Z-0326-2016",
      "product_description": "NxStage System One S Cycler (High Permeability Hemodialysis System)  Model no. NX1000-5",
      "product_quantity": "323 units",
      "reason_for_recall": "Ultrafiltration (UF) Volume software error inaccurate fluid removal",
      "recall_initiation_date": "20151029",
      "center_classification_date": "20151123",
      "termination_date": "20190429",
      "report_date": "20151202",
      "code_info": "Software versions 4.9 and 4.10"
    }
  ]
}