{
  "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-1861-2014",
      "product_description": "NxStage Dialysate Sack (SAK) with Concentrate  for Use with PureFlow SL  REF: SAK-407  Lactate 40, Potassium 1, Sodium 140, Calcium 3, Magnesium 1,   Chloride 105, Glucose (mg/dL) 100  Batch Size (liters) 50",
      "product_quantity": "91 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 code:  40179074"
    }
  ]
}