{
  "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-0825-2021",
      "product_description": "NaturaLyte Liquid Acid concentrate drums, Model Number 13-2251-0 - 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": "592 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: 20LXAC070  20LXAC103  20NXAC021  20LXAC100  20LXAC026  20LXAC027  20LXAC028  20LXAC029  20LXAC065  20LXAC067  20LXAC071  20NXAC001  20NXAC019  20NXAC020  20NXAC029    Additional affected lots as of 3/17/21: 20LXAC103  20LXAC082  20LXAC025  20LXAC081  20LXAC083"
    }
  ]
}