{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
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    }
  },
  "results": [
    {
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      "city": "Lenoir",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
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        "substance_name": [
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        "is_original_packager": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "96481",
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      "address_1": "1245 Blowing Rock Blvd",
      "address_2": "N/A",
      "postal_code": "28645-3618",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
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      "recall_number": "D-0303-2025",
      "product_description": "8.4% Sodium Bicarbonate Injection, USP, 50 mEq/50 mL (1 mEq/mL), 25 x 50 mL Single Dose Vials per carton, For Intravenous Use Only, Rx Only, Manufactured by: Exela Pharma Sciences, LLC, Lenoir, NC 28645. NDC Inner Vial: 51754-5001-1; NDC Carton: 51754-5001-4",
      "product_quantity": "103,950 vials",
      "reason_for_recall": "Lack of Assurance of Sterility",
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      "code_info": "Lots: 10006417 and 10006418, Exp. 11/30/2026"
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}