{
  "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": [
          "NDA016673"
        ],
        "brand_name": [
          "DEXTROSE"
        ],
        "generic_name": [
          "DEXTROSE MONOHYDRATE"
        ],
        "manufacturer_name": [
          "Baxter Healthcare Corporation"
        ],
        "product_ndc": [
          "0338-0017",
          "0338-0023"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "DEXTROSE MONOHYDRATE"
        ],
        "rxcui": [
          "1795477",
          "1795480",
          "1795481",
          "1795607",
          "1795609",
          "1795610",
          "1795612",
          "1795616",
          "1795618"
        ],
        "spl_id": [
          "31bb4a5f-733e-4354-9fbf-138dede4db0f"
        ],
        "spl_set_id": [
          "3bb406a9-f5cb-403a-b1bb-5c4facbea3d5"
        ],
        "package_ndc": [
          "0338-0017-10",
          "0338-0017-41",
          "0338-0017-11",
          "0338-0017-31",
          "0338-0017-48",
          "0338-0017-18",
          "0338-0017-38",
          "0338-0017-02",
          "0338-0017-03",
          "0338-0017-04",
          "0338-0023-02",
          "0338-0023-03",
          "0338-0023-04"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "LX22YL083G"
        ]
      },
      "product_type": "Drugs",
      "event_id": "67092",
      "recalling_firm": "Baxter Healthcare Corp.",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide, Puerto Rico, Singapore, Saudi Arabia and United Arab Emirates.",
      "recall_number": "D-1162-2014",
      "product_description": "5% Dextrose Injection, USP, 100 mL Single dose VIAFLEX plastic containers, Rx only, Baxter Healthcare Corporation, Deerfield, IL  60015 USA, Product code 2B0089, NDC 0338-0017-38.",
      "product_quantity": "105,216 containers",
      "reason_for_recall": "Presence of Paticulate Matter; Baxter is issuing a voluntary recall for these IV solutions due to particulate matter found in the solution identified as polyester and cotton fibers, adhesive-like mixture, polyacetal particles, thermally degraded PVC, black polypropylene and human hair embedded in the plastic bag",
      "recall_initiation_date": "20131121",
      "center_classification_date": "20140314",
      "termination_date": "20160921",
      "report_date": "20140326",
      "code_info": "Lot #: P285288, Exp 11/13",
      "more_code_info": ""
    }
  ]
}