{
  "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": "2026-07-08",
    "results": {
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      "status": "Terminated",
      "city": "Fort Worth",
      "state": "TX",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "90062",
      "recalling_firm": "Monarch PCM, LLC",
      "address_1": "7333 Jack Newell Blvd N Ste 100",
      "address_2": "N/A",
      "postal_code": "76118-7151",
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      "distribution_pattern": "TN only",
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      "product_description": "Phenobarbital Elixir, USP 20 mg/5 mL, 1 Pint (473 mL) bottles,  Rx Only,  Manufactured for: Westminster Pharmaceuticals, LLC Tampa, FL 33624, NDC 69367-172-16",
      "product_quantity": "15,730 bottles",
      "reason_for_recall": "Does Not Meet USP or OTC Monograph: Product exceeds USP specification for alcohol content",
      "recall_initiation_date": "20220414",
      "center_classification_date": "20220517",
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      "code_info": "Lot #: 20FP1569 Exp. Date 08/2022; 21FP1674 Exp. Date 02/2023; 21FP1831 Exp. Date 08/2023",
      "more_code_info": ""
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}