{
  "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": [
    {
      "status": "Terminated",
      "city": "Moon Township",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "71750",
      "recalling_firm": "GlaxoSmithkline Consmer Healthcare",
      "address_1": "1000 GSK Drive",
      "address_2": "N/A",
      "postal_code": "15108",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide, Puerto Rico & Taiwan",
      "recall_number": "D-1320-2015",
      "product_description": "biotene PBF Toothpaste (Plaque-Biofilm Loosening Formula), a) 4.3 oz. (121.9 g) tubes, (NDC 0135-0559-01), biotene¿ PBF Paste, b) 4.5 oz.(127.6 g) tubes, (NDC 0135-0490-02), Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108",
      "product_quantity": "50,860 tubes",
      "reason_for_recall": "Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.",
      "recall_initiation_date": "20150715",
      "center_classification_date": "20150811",
      "termination_date": "20170419",
      "report_date": "20150819",
      "code_info": "Lot #     a)    Z3M191, Exp 10/15  Z4C081, Exp 02/16  Z4H171, Exp 07/16    b)    Z2K301, Exp 10/15  Z3D181, Exp 04/16"
    }
  ]
}