{
  "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": "2026-09-02",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Morgantown",
      "state": "WV",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
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        "generic_name": [
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        "product_ndc": [
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        "route": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "99483",
      "recalling_firm": "Mylan Pharmaceuticals Inc",
      "address_1": "3711 Collins Ferry Rd",
      "address_2": "",
      "postal_code": "26505-2362",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide.",
      "recall_number": "D-0774-2026",
      "product_description": "Acamprosate Calcium, Delayed-Release Tablets, 333 mg, 180 tablets bottles, Rx only, Mylan Pharmaceuticals Inc., Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 266505, NDC 0378-6333-80.",
      "product_quantity": "",
      "reason_for_recall": "Failed Dissolution Specifications",
      "recall_initiation_date": "20260724",
      "center_classification_date": "20260819",
      "report_date": "20260826",
      "code_info": "Lot# 3227809; Expiry:10/2026; NDC #: 0378-6333-80",
      "more_code_info": ""
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}