{
  "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": {
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      "state": "TN",
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      "classification": "Class III",
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      "product_type": "Drugs",
      "event_id": "92535",
      "recalling_firm": "AVKARE LLC",
      "address_1": "615 N 1st St",
      "address_2": "N/A",
      "postal_code": "38478-2403",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
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      "recall_number": "D-0875-2023",
      "product_description": "Tranexamic Acid USP Tablets, 650 mg, 30 tablets (3X10) Unit Dose, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478, NDC 50268-772-13",
      "product_quantity": "592 cartons",
      "reason_for_recall": "Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.",
      "recall_initiation_date": "20230613",
      "center_classification_date": "20230615",
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      "code_info": "Lot: 44286 Exp. 02/2025"
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}