{
  "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": "2026-03-18",
    "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": "90367",
      "recalling_firm": "Fresenius Medical Care Holdings, Inc.",
      "address_1": "920 Winter St Bld 950",
      "address_2": "",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of Pennsylvania.",
      "recall_number": "Z-1303-2022",
      "product_description": "Optiflux 200NRe Dialyzer Finished Assy., Model no. 0500320E",
      "product_quantity": "19 cases",
      "reason_for_recall": "Dialyzers were distributed after being exposed to cold temperatures which exceeded the low-temperature range in the firm's standard operating procedure.",
      "recall_initiation_date": "20220504",
      "center_classification_date": "20220630",
      "termination_date": "20240506",
      "report_date": "20220706",
      "code_info": "UDI-DI (GTIN): (01)00840861100163 Lot 22AU04017",
      "more_code_info": ""
    }
  ]
}