{
  "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": [
    {
      "status": "Terminated",
      "city": "Canonsburg",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "91038",
      "recalling_firm": "Viatris Inc",
      "address_1": "1000 Mylan Blvd",
      "address_2": "N/A",
      "postal_code": "15317-5853",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0063-2023",
      "product_description": "Carvedilol Tablets, USP, 25 mg, 500-count bottles, Rx Only, Mfg: Mylan Pharmaceuticals Inc. Morgantown, WV 36505, Made in India, NDC 0378-3634-05",
      "product_quantity": "2,794 bottles",
      "reason_for_recall": "Failed Tablet/Capsule Specifications: Tablets exceeds specification for weight and thickness.",
      "recall_initiation_date": "20221021",
      "center_classification_date": "20221116",
      "termination_date": "20230713",
      "report_date": "20221123",
      "code_info": "Lot #: 3150116, Exp 2/2025"
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}