{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73387",
      "recalling_firm": "Fresenius Medical Care Renal Therapies Group, LLC",
      "address_1": "920 Winter St",
      "address_2": "N/A",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution including states of: AZ, CA, CT, DC, GA, IL, IN, MI, MN, MO, MS, NY, OH, PA, SC, SD, TX, and WA.",
      "recall_number": "Z-1324-2016",
      "product_description": "Fresenius Hemoflow F3 Dialyzer  Part Number: 0520165A    Indicated for Acute and Chronic Hemodialysis",
      "product_quantity": "1,650 units",
      "reason_for_recall": "Dialyzer header leak due to possible improper torque",
      "recall_initiation_date": "20160226",
      "center_classification_date": "20160405",
      "termination_date": "20170626",
      "report_date": "20160413",
      "code_info": "Lot Number: 15KU04011  Exp. Date : 08/31/2013",
      "more_code_info": ""
    }
  ]
}