{
  "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": [
    {
      "status": "Terminated",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81598",
      "recalling_firm": "Fresenius Medical Care Renal Therapies Group, LLC",
      "address_1": "920 Winter St",
      "address_2": "",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide",
      "recall_number": "Z-0658-2019",
      "product_description": "Optiflux F160NR Capillary High Flux Dialyzer Single Use Only, Product Code 0500316E",
      "product_quantity": "9,097 cs x 12 units each",
      "reason_for_recall": "Potential for external blood leaks from the dialyzer header",
      "recall_initiation_date": "20181105",
      "center_classification_date": "20181220",
      "termination_date": "20230417",
      "report_date": "20181226",
      "code_info": "Lot Numbers: 18HU06016, 18HU06017, 18HU06018 and 18HU06019",
      "more_code_info": ""
    }
  ]
}