{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
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        ],
        "brand_name": [
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        "generic_name": [
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        "product_type": [
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        "rxcui": [
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      "product_type": "Drugs",
      "event_id": "70695",
      "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 and Singapore",
      "recall_number": "D-0429-2015",
      "product_description": "0.9% Sodium Chloride Injection, USP, 50 mL, VIAFLEX Plastic Container Multi Pack, Rx Only, Baxter Healthcare Corporation, Deerfield, IL , Product code 2B1308, NDC 0338-0049-31",
      "product_quantity": "196,128 containers",
      "reason_for_recall": "Lack of Assurance of Sterility; increased complaints received for leaks",
      "recall_initiation_date": "20150323",
      "center_classification_date": "20150331",
      "termination_date": "20161020",
      "report_date": "20150408",
      "code_info": "Product code: 2B1308; Lot#: P316497, exp date: 10/2015"
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}