{
  "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": "2026-04-29",
    "results": {
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      "city": "Dublin",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
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      "address_2": "N/A",
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      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide.",
      "recall_number": "D-0485-2026",
      "product_description": "Memantine Hydrochloride Extended-Release, Capsules, 7 mg, 100 Capsules (10 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC  0904-6734-61",
      "product_quantity": "N/A",
      "reason_for_recall": "Failed Dissolution Specifications",
      "recall_initiation_date": "20260324",
      "center_classification_date": "20260417",
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      "code_info": "Lot # N02425, Exp Date: 05/31/2027."
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}