{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "country": "United States",
      "city": "Wixom",
      "address_1": "30142 S. Wixom Rd.",
      "reason_for_recall": "A subassembly component (dextrose bag) within this case product contained small amounts of sodium bicarbonate from a prior batch.",
      "address_2": "",
      "product_quantity": "139",
      "code_info": "Lot 28562-0220171",
      "center_classification_date": "20180514",
      "distribution_pattern": "US Distribution to the state of NY",
      "state": "MI",
      "product_description": "DriSate¿ Product Code DR-145    The acid concentrate powders and liquids are indicated for use in acute and chronic hemodialysis and to be used with the appropriate hemodialysis machine/monitor and bicarbonate concentrate.",
      "report_date": "20180523",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Rockwell Medical, Inc",
      "recall_number": "Z-1869-2018",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "79878",
      "termination_date": "20181001",
      "more_code_info": "",
      "recall_initiation_date": "20180407",
      "postal_code": "48393-3440",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}