{
  "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,
      "limit": 1,
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    }
  },
  "results": [
    {
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      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
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          "ALLOPURINOL"
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        ],
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          "0355111730019"
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        "pharm_class_epc": [
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        ],
        "pharm_class_moa": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "94781",
      "recalling_firm": "Dr. Reddy's Laboratories, Inc.",
      "address_1": "107 College Rd E",
      "address_2": "N/A",
      "postal_code": "08540-6623",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "IL, MS, OH",
      "recall_number": "D-0583-2024",
      "product_description": "Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA, NDC 55111-730-01.",
      "product_quantity": "20,520 units",
      "reason_for_recall": "Presence of foreign substance.",
      "recall_initiation_date": "20240607",
      "center_classification_date": "20240703",
      "termination_date": "20251222",
      "report_date": "20240710",
      "code_info": "L2300594"
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}