{
  "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-1749-2020",
      "product_description": "Fresenius 2008T BlueStar Hemodialysis Machine    Part Number Description:  191124 2008T HD SYS. CDX BLUEST AR;  191126 2008T HD SYS. CDX W/BIBAG BLUEST AR;  191128 2008T HD SYS. W/O CDX BLUEST AR;  191130 2008T HD SYS. W/O CDX W/BIBAG BLUEST AR",
      "product_quantity": "15,342",
      "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"
    }
  ]
}