{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Waltham",
      "address_1": "920 Winter St",
      "reason_for_recall": "Power Logic Board Fail Message on the 2008T BlueStar Machine with software version 2.72.",
      "address_2": "",
      "product_quantity": "257 units",
      "code_info": "Software v.2.72",
      "center_classification_date": "20190531",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "MA",
      "product_description": "2008T BlueStar Machine Software v.2.72-Hemodialysis machine   Model Number: 191126 - Product Usage: The 2008T hemodialysis machine is indicated for acute and chronic dialysis therapy in a healthcare facility.",
      "report_date": "20190612",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Fresenius Medical Care Renal Therapies Group, LLC",
      "recall_number": "Z-1699-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82729",
      "termination_date": "20190830",
      "more_code_info": "",
      "recall_initiation_date": "20190403",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}