{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lawrence",
      "address_1": "350 Merrimack St",
      "reason_for_recall": "Certain lots were mislabeled with incorrect product number.",
      "address_2": "",
      "product_quantity": "1998 units",
      "code_info": "Lot Number: Q1811792  Exp Date: 11/1/2020",
      "center_classification_date": "20190602",
      "distribution_pattern": "US Nationwide Distribution - AZ, CA, DC, FL, GA, IL, IN, MI, NC, NH, NV, PA, TX & VA",
      "state": "MA",
      "product_description": "NxStage PureFlow B Solution, REF RFP-400, M535RFP4000    Product NxStage PureFlow B Solution is indicated for use with renal  replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "NxStage Medical, Inc.",
      "recall_number": "Z-1706-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82693",
      "termination_date": "20200608",
      "more_code_info": "",
      "recall_initiation_date": "20190411",
      "postal_code": "01843-1748",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}