{
  "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": "Terminated",
      "city": "Phoenix",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85695",
      "recalling_firm": "Diasol, Inc",
      "address_1": "310 S 43rd Ave Ste B",
      "address_2": "",
      "postal_code": "85009-4606",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S.: CA    O.U.S.:None",
      "recall_number": "Z-2402-2020",
      "product_description": "DIASOL 1000225-10-DEX100 LIQUID ACID CONCENTRATE FOR BICARBONATE DIALYSIS",
      "product_quantity": "212 Cases of 4 gallons each",
      "reason_for_recall": "Incorrect labeling of dialysate concentration for hemodialysis.",
      "recall_initiation_date": "20200430",
      "center_classification_date": "20200618",
      "termination_date": "20240528",
      "report_date": "20200624",
      "code_info": "Model Number: 100225-10-DEX100 Gallons  Unique Device Identifier (UDI): B467100225101004 and B4671000225101004  Lot codes if applicable: PHQ03041/030920",
      "more_code_info": ""
    }
  ]
}