{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Bellmawr",
      "address_1": "136 Harding Ave",
      "reason_for_recall": "Labeling: Label Mixup; potentially mislabeled",
      "address_2": "",
      "product_quantity": "unknown",
      "code_info": "Lot # 70926A; Exp. 11/17  Lot # 70981A; Exp. 01/18  Lot # H15A59; Exp. 08/18",
      "center_classification_date": "20170822",
      "distribution_pattern": "Nationwide",
      "state": "NJ",
      "product_description": "Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6145-10",
      "report_date": "20170830",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "C. O. Truxton",
      "recall_number": "D-1112-2017",
      "initial_firm_notification": "Press Release",
      "product_type": "Drugs",
      "event_id": "77082",
      "termination_date": "20180911",
      "more_code_info": "",
      "recall_initiation_date": "20170420",
      "postal_code": "08031-2412",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}