{
  "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 II",
      "openfda": {
        "application_number": [
          "NDA018609"
        ],
        "brand_name": [
          "HEPARIN SODIUM IN SODIUM CHLORIDE"
        ],
        "generic_name": [
          "HEPARIN SODIUM"
        ],
        "manufacturer_name": [
          "Baxter Healthcare Corporation"
        ],
        "product_ndc": [
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          "0338-0431",
          "0338-0433",
          "0338-0428"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "HEPARIN SODIUM"
        ],
        "rxcui": [
          "1658690",
          "1658692"
        ],
        "spl_id": [
          "68b37381-6db4-4ac0-ba6b-3204add02665"
        ],
        "spl_set_id": [
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        ],
        "package_ndc": [
          "0338-0431-03",
          "0338-0433-04",
          "0338-0424-18",
          "0338-0428-12"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "ZZ45AB24CA"
        ]
      },
      "product_type": "Drugs",
      "event_id": "69634",
      "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-0276-2015",
      "product_description": "Heparin Sodium in 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx only, Manufactured for Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015 by Baxter Healthcare Corporation 250 Road 144 Jayuya, Puerto Rico, 00664, NDC 0338-0431-03",
      "product_quantity": "127,746 Viaflex Plus Container",
      "reason_for_recall": "Subpotent Drug: Heparin raw material was found to have low potency",
      "recall_initiation_date": "20141030",
      "center_classification_date": "20141124",
      "termination_date": "20160922",
      "report_date": "20141203",
      "code_info": "Lot #: N003061; N003079; and N003087, Exp 2/29/2016",
      "more_code_info": ""
    }
  ]
}