{
  "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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    {
      "status": "Terminated",
      "city": "Canonsburg",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "90091",
      "recalling_firm": "Viatris Inc",
      "address_1": "1000 Mylan Blvd",
      "address_2": "N/A",
      "postal_code": "15317-5853",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "Product was distributed nationwide in the USA",
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      "product_description": "Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co, Division of Fizer Inc, NY, NY  10017, NDC 0009-0068-07.",
      "product_quantity": "110 bottles",
      "reason_for_recall": "Failed Dissolution Specifications: low out of specification results for dissolution.",
      "recall_initiation_date": "20220428",
      "center_classification_date": "20220506",
      "termination_date": "20230713",
      "report_date": "20220518",
      "code_info": "Lot #: DX7983, exp. date 02/28/2023"
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