{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Little Rock",
      "address_1": "8821 Knoedl Ct",
      "reason_for_recall": "Lack of sterility assurance",
      "address_2": "",
      "product_quantity": "660 bags",
      "code_info": "Lot #: 20170509@6, Exp 6/23/2017; 20170519@35, Exp 7/3/2017; 20170523@22, Exp 7/7/2017; 20170525@9, Exp 7/9/2017; 20170605@49, Exp 7/20/2017; 20170605@9, Exp 7/20/2017",
      "center_classification_date": "20170713",
      "distribution_pattern": "LA, PA, NY, WI",
      "state": "AR",
      "product_description": "Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 mMol (22 mEq K+) Total Approximate Volume 255 mL,  Rx only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0841-40",
      "report_date": "20170719",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "SCA Pharmaceuticals",
      "recall_number": "D-0977-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "77600",
      "termination_date": "20190403",
      "more_code_info": "",
      "recall_initiation_date": "20170621",
      "postal_code": "72205-4600",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}