{
  "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": "Ongoing",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85310",
      "recalling_firm": "Fresenius Medical Care Holdings, Inc.",
      "address_1": "920 Winter St Bld 950",
      "address_2": "N/A",
      "postal_code": "02451-1521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign: Canada, Curaca, Guam",
      "recall_number": "Z-1748-2020",
      "product_description": "Fresenius 2008T Hemodialysis Machine:  Part Number Description  190573 2008T HEMODIAL YSIS SYS. OLC/DIASAFE PLUS;  190713 2008T HEMODIAL YSIS SYS., with CDX;  190766 2008T HEMODIAL YSIS SYSTEM W/BIBAG;  190858 2008T HEMODIAL YSIS SYSTEM WITHOUT CDX;  190895 2008T GEN 2 BIBAG WITHOUT CDX;  190908 2008T HD System With CDX, CAN",
      "product_quantity": "101,463",
      "reason_for_recall": "A \"Remove USB Device 2\" false alarm may be displayed when no USB device or a non-powered USB device is connected to the USB port on the rear of the machine",
      "recall_initiation_date": "20200312",
      "center_classification_date": "20200420",
      "report_date": "20200429",
      "code_info": "All serial numbers"
    }
  ]
}