{
  "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": "Kirkland",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class III",
      "openfda": {
        "application_number": [
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        ],
        "brand_name": [
          "SODIUM IODIDE I 131 DIAGNOSTIC"
        ],
        "generic_name": [
          "SODIUM IODIDE I 131"
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        "manufacturer_name": [
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        "product_ndc": [
          "65174-461"
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        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
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        "substance_name": [
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        "spl_id": [
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        ],
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "73586",
      "recalling_firm": "Jubilant Draximage Inc",
      "address_1": "16751 Rte Trans-Canada",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0812-2016",
      "product_description": "SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC, Canada, NDC 65174-461-05",
      "product_quantity": "90 vials (450 capsules)",
      "reason_for_recall": "Labeling: Label Error on Declared Strength",
      "recall_initiation_date": "20160311",
      "center_classification_date": "20160406",
      "termination_date": "20170807",
      "report_date": "20160413",
      "code_info": "Lot Number 1670123; Exp 04/16",
      "more_code_info": ""
    }
  ]
}