{
  "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": "Waltham",
      "address_1": "920 Winter St",
      "reason_for_recall": "Updated Instructions for Use: Bloodline connections not tightened per instructions in the operator's manual may  disconnect and lead to blood loss",
      "address_2": "",
      "product_quantity": "24,202 cases",
      "code_info": "All lot codes",
      "center_classification_date": "20131108",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the country of Canada.",
      "state": "MA",
      "product_description": "Combiset Blood Line with BVM for Hemodialysis use  Catalog Number: 03-2965-9.    Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.",
      "report_date": "20131120",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Fresenius Medical Care Holdings, Inc.",
      "recall_number": "Z-0185-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65739",
      "termination_date": "20210211",
      "more_code_info": "",
      "recall_initiation_date": "20130829",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}