{
  "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,
      "total": 1
    }
  },
  "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": "a)  Lot # 70989A; Exp. 02/18, Lot # 70973A; Exp. 01/18    b)  Lot # 70973A; Exp. 01/18, Lot # H15A76; Exp. 02/18, Lot # 71346A; Exp. 12/19, Lot # 70989A; Exp. 02/18",
      "center_classification_date": "20170822",
      "distribution_pattern": "Nationwide",
      "state": "NJ",
      "product_description": "Phenobarbital Tablets USP, 100 mg, a) 100 count bottles (NDC 0463-6152-01), b) 1000 count bottles (NDC 0163-6152-10), Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031",
      "report_date": "20170830",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "C. O. Truxton",
      "recall_number": "D-1114-2017",
      "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"
    }
  ]
}