{
  "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": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {
        "application_number": [
          "NDA020047"
        ],
        "brand_name": [
          "DEXTROSE"
        ],
        "generic_name": [
          "DEXTROSE MONOHYDRATE"
        ],
        "manufacturer_name": [
          "Baxter Healthcare Corporation"
        ],
        "product_ndc": [
          "0338-0719"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "DEXTROSE MONOHYDRATE"
        ],
        "rxcui": [
          "237656"
        ],
        "spl_id": [
          "aa64f648-e931-4a99-9b81-791a3827272c"
        ],
        "spl_set_id": [
          "0332f34a-7038-47cc-ba59-d55cad6b73ca"
        ],
        "package_ndc": [
          "0338-0719-06"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "LX22YL083G"
        ]
      },
      "product_type": "Drugs",
      "event_id": "72816",
      "recalling_firm": "Baxter Healthcare Corp.",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0958-2016",
      "product_description": "Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For Direct Infusion, Must Be Diluted, Rx Only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 0338-0719-06",
      "product_quantity": "28,080 VIAFLEX Plastic Containers",
      "reason_for_recall": "Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.",
      "recall_initiation_date": "20151215",
      "center_classification_date": "20160606",
      "termination_date": "20220415",
      "report_date": "20160615",
      "code_info": "Lot # C985150; Exp.  07/16"
    }
  ]
}