{
  "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": "Lawrence",
      "address_1": "350 Merrimack Street",
      "reason_for_recall": "Mislabeled product.",
      "address_2": "",
      "product_quantity": "969 cases (2 bags per case)",
      "code_info": "Lot Number: F113662",
      "center_classification_date": "20140224",
      "distribution_pattern": "US Distribution including the states of NY, TX, ID, AR, CA and AL",
      "state": "MA",
      "product_description": "NxStage PureFlow-B Solution; Model/Catalog Number: RFP-401.  Product is packaged in a case containing two individual 5L bags.      The NxStage PureFlow-B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.",
      "report_date": "20140305",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "NxStage Medical, Inc.",
      "recall_number": "Z-1073-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67405",
      "termination_date": "20140829",
      "more_code_info": "",
      "recall_initiation_date": "20140124",
      "postal_code": "01843-1748",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}