{
  "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": [
    {
      "status": "Terminated",
      "city": "Lawrence",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68354",
      "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 - USA (nationwide) and Internationally to France, Netherlands, Spain, Sweden, and the UK.",
      "recall_number": "Z-1858-2014",
      "product_description": "NxStage Dialysate Sack (SAK) with Concentrate  for Use with PureFlow SL  REF: SAK-305  Lactate 45, Potassium 1, Sodium 140, Calcium 3, Magnesium 1  Chloride 100, Glucose (mg/dL) 100  Batch Size (liters) 40",
      "product_quantity": "2839 cases",
      "reason_for_recall": "SAK Dialysate Concentrate contain aluminum levels which exceed internal product specification",
      "recall_initiation_date": "20140514",
      "center_classification_date": "20140624",
      "termination_date": "20170313",
      "report_date": "20140702",
      "code_info": "Lot codes:  40179026  3057901  3047930"
    }
  ]
}