{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Morgantown",
      "address_1": "781 Chestnut Ridge Rd",
      "reason_for_recall": "Failed Dissolution Specifications",
      "address_2": "",
      "product_quantity": "24,176 bottles (1,450,560 tablets)",
      "code_info": "Code: 0378-5022-91 Lot: 3065878; Exp. 04/17",
      "center_classification_date": "20170524",
      "distribution_pattern": "Nationwide",
      "state": "WV",
      "product_description": "Alprazolam Extended-release Tablets, USP, 1 mg,  60-count bottle, Rx Only, Manufactured and Distributed by: Mylan Pharmaceuticals Inc.,  Morgantown, WV 26505 U.S.A.,  NDC 0378-5022-91",
      "report_date": "20170531",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Mylan Pharmaceuticals Inc.",
      "recall_number": "D-0706-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "76922",
      "termination_date": "20170712",
      "more_code_info": "",
      "recall_initiation_date": "20160622",
      "postal_code": "26505-2730",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}