{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Philadelphia",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "89551",
      "recalling_firm": "Lannett Company, Inc.",
      "address_1": "9000 State Rd",
      "address_2": "N/A",
      "postal_code": "19136-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed nationwide in the USA.",
      "recall_number": "D-0558-2022",
      "product_description": "Diazepam Oral Solution (Concentrate), 25 mg per 5 mL (5 mg/mL), 30 mL BOTTLE and DROPPER, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1768-36.",
      "product_quantity": "23,598 bottles",
      "reason_for_recall": "Failed Impurities/Degradation Specifications: Out of specification results for related substances.",
      "recall_initiation_date": "20220209",
      "center_classification_date": "20220214",
      "termination_date": "20230501",
      "report_date": "20220223",
      "code_info": "Lot #: 2664A, 2664B, Exp. date 07/2022; 2874A, 2874B, Exp. date 01/2023"
    }
  ]
}