{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Morgantown",
      "address_1": "781 Chestnut Ridge Rd",
      "reason_for_recall": "cGMP Deviations; cleaning process for equipment used to manufacture the specified batches was not followed according to procedure",
      "address_2": "",
      "product_quantity": "25,488 bottles",
      "code_info": "Lot Numbers# 3083005, 3083006, 3086121, and 3086122, exp Jan 2019",
      "center_classification_date": "20180517",
      "distribution_pattern": "Product was distributed throughout United States",
      "state": "WV",
      "product_description": "Amlodipine and Benazapril HCL Capsules, USP, 5 mg/10 mg, 100 count bottles, Mylan Pharmaceuticals, Inc., Morgantown, WV --- NDC 0378-6896-01",
      "report_date": "20180523",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Mylan Pharmaceuticals Inc.",
      "recall_number": "D-0819-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "79957",
      "termination_date": "20190620",
      "more_code_info": "",
      "recall_initiation_date": "20180424",
      "postal_code": "26505-2730",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}