{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Houston",
      "address_1": "9265 Kirby Dr",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "address_2": "",
      "product_quantity": "72 units",
      "code_info": "Lot #: 5/23/17 1404 299-92625P, BUD: 8/21/2017; 5/26/2017 1250 297-92625P, BUD 8/24/2017.",
      "center_classification_date": "20170707",
      "distribution_pattern": "Nationwide with the United States",
      "state": "TX",
      "product_description": "Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 20 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-926-25",
      "report_date": "20170719",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Advanced Pharma Inc.",
      "recall_number": "D-0954-2017",
      "initial_firm_notification": "Press Release",
      "product_type": "Drugs",
      "event_id": "77595",
      "termination_date": "20171206",
      "more_code_info": "",
      "recall_initiation_date": "20170622",
      "postal_code": "77054-2520",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}