{
  "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": "86855",
      "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": "US Nationwide distribution.",
      "recall_number": "Z-0826-2021",
      "product_description": "NaturaLyte Liquid Acid concentrate drums, Model Number 13-3251-9 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.",
      "product_quantity": "230 drums",
      "reason_for_recall": "The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.",
      "recall_initiation_date": "20201107",
      "center_classification_date": "20210111",
      "report_date": "20210120",
      "code_info": "Lot Numbers: 20LXAC024  20LXAC072  20LXAC073  20LXAC085  20NXAC017  20NXAC030  20LXAC074  20LXAC023  20LXAC104    Additional affected lots as of 3/17/21: 20LXAC066  20LXAC089"
    }
  ]
}